Ecoer Logo
VOTING POWER100.00%
DOWNVOTE POWER100.00%
RESOURCE CREDITS100.00%
REPUTATION PROGRESS68.37%
Net Worth
0.037USD
STEEM
0.000STEEM
SBD
0.000SBD
Effective Power
5.007SP
├── Own SP
0.633SP
└── Incoming Deleg
+4.374SP

Detailed Balance

STEEM
balance
0.000STEEM
market_balance
0.000STEEM
savings_balance
0.000STEEM
reward_steem_balance
0.000STEEM
STEEM POWER
Own SP
0.633SP
Delegated Out
0.000SP
Delegation In
4.374SP
Effective Power
5.007SP
Reward SP (pending)
0.000SP
SBD
sbd_balance
0.000SBD
sbd_conversions
0.000SBD
sbd_market_balance
0.000SBD
savings_sbd_balance
0.000SBD
reward_sbd_balance
0.000SBD
{
  "balance": "0.000 STEEM",
  "savings_balance": "0.000 STEEM",
  "reward_steem_balance": "0.000 STEEM",
  "vesting_shares": "1029.672820 VESTS",
  "delegated_vesting_shares": "0.000000 VESTS",
  "received_vesting_shares": "7113.986986 VESTS",
  "sbd_balance": "0.000 SBD",
  "savings_sbd_balance": "0.000 SBD",
  "reward_sbd_balance": "0.000 SBD",
  "conversions": []
}

Account Info

namedvendetta
id383783
rank874,364
reputation-14004204351
created2017-09-25T19:25:36
recovery_accountsteem
proxyNone
post_count3
comment_count0
lifetime_vote_count0
witnesses_voted_for0
last_post2017-09-28T15:38:12
last_root_post2017-09-28T15:38:12
last_vote_time1970-01-01T00:00:00
proxied_vsf_votes0, 0, 0, 0
can_vote1
voting_power0
delayed_votes0
balance0.000 STEEM
savings_balance0.000 STEEM
sbd_balance0.000 SBD
savings_sbd_balance0.000 SBD
vesting_shares1029.672820 VESTS
delegated_vesting_shares0.000000 VESTS
received_vesting_shares7113.986986 VESTS
reward_vesting_balance0.000000 VESTS
vesting_balance0.000 STEEM
vesting_withdraw_rate0.000000 VESTS
next_vesting_withdrawal1969-12-31T23:59:59
withdrawn0
to_withdraw0
withdraw_routes0
savings_withdraw_requests0
last_account_recovery1970-01-01T00:00:00
reset_accountnull
last_owner_update1970-01-01T00:00:00
last_account_update2017-09-25T19:49:57
minedNo
sbd_seconds0
sbd_last_interest_payment1970-01-01T00:00:00
savings_sbd_last_interest_payment1970-01-01T00:00:00
{
  "id": 383783,
  "name": "dvendetta",
  "owner": {
    "weight_threshold": 1,
    "account_auths": [],
    "key_auths": [
      [
        "STM5bxVB5QG4YVD9URbKvb3FEerE5o8QEmKWYSoMyDonFmVndgy11",
        1
      ]
    ]
  },
  "active": {
    "weight_threshold": 1,
    "account_auths": [],
    "key_auths": [
      [
        "STM6VoUYAa3yiU7bfGfuEM1fM1yFARq8ajWyE4MJsqpNUnLwyv8Wu",
        1
      ]
    ]
  },
  "posting": {
    "weight_threshold": 1,
    "account_auths": [],
    "key_auths": [
      [
        "STM7A1F2U855xSJU5Zjw7HzGVP4xvFUnK7WN8dcKj27pWumD1j5WU",
        1
      ]
    ]
  },
  "memo_key": "STM7Vi4E9CP4Uk1sdbAnpaN78j7Bn6wpBanACyU9xbqinptGdkDcm",
  "json_metadata": "{\"profile\":{\"cover_image\":\"https://s26.postimg.org/h8kvhs23t/Le-magnifique-ciel-de-nuit-en-hiver-en-_Nouvelle-.jpg\",\"profile_image\":\"https://s26.postimg.org/pgmt2ru09/logodbassah.png\",\"name\":\"Moussa\"}}",
  "posting_json_metadata": "{\"profile\":{\"cover_image\":\"https://s26.postimg.org/h8kvhs23t/Le-magnifique-ciel-de-nuit-en-hiver-en-_Nouvelle-.jpg\",\"profile_image\":\"https://s26.postimg.org/pgmt2ru09/logodbassah.png\",\"name\":\"Moussa\"}}",
  "proxy": "",
  "last_owner_update": "1970-01-01T00:00:00",
  "last_account_update": "2017-09-25T19:49:57",
  "created": "2017-09-25T19:25:36",
  "mined": false,
  "recovery_account": "steem",
  "last_account_recovery": "1970-01-01T00:00:00",
  "reset_account": "null",
  "comment_count": 0,
  "lifetime_vote_count": 0,
  "post_count": 3,
  "can_vote": true,
  "voting_manabar": {
    "current_mana": "8143659806",
    "last_update_time": 1779061536
  },
  "downvote_manabar": {
    "current_mana": 2035914951,
    "last_update_time": 1779061536
  },
  "voting_power": 0,
  "balance": "0.000 STEEM",
  "savings_balance": "0.000 STEEM",
  "sbd_balance": "0.000 SBD",
  "sbd_seconds": "0",
  "sbd_seconds_last_update": "1970-01-01T00:00:00",
  "sbd_last_interest_payment": "1970-01-01T00:00:00",
  "savings_sbd_balance": "0.000 SBD",
  "savings_sbd_seconds": "0",
  "savings_sbd_seconds_last_update": "1970-01-01T00:00:00",
  "savings_sbd_last_interest_payment": "1970-01-01T00:00:00",
  "savings_withdraw_requests": 0,
  "reward_sbd_balance": "0.000 SBD",
  "reward_steem_balance": "0.000 STEEM",
  "reward_vesting_balance": "0.000000 VESTS",
  "reward_vesting_steem": "0.000 STEEM",
  "vesting_shares": "1029.672820 VESTS",
  "delegated_vesting_shares": "0.000000 VESTS",
  "received_vesting_shares": "7113.986986 VESTS",
  "vesting_withdraw_rate": "0.000000 VESTS",
  "next_vesting_withdrawal": "1969-12-31T23:59:59",
  "withdrawn": 0,
  "to_withdraw": 0,
  "withdraw_routes": 0,
  "curation_rewards": 0,
  "posting_rewards": 0,
  "proxied_vsf_votes": [
    0,
    0,
    0,
    0
  ],
  "witnesses_voted_for": 0,
  "last_post": "2017-09-28T15:38:12",
  "last_root_post": "2017-09-28T15:38:12",
  "last_vote_time": "1970-01-01T00:00:00",
  "post_bandwidth": 0,
  "pending_claimed_accounts": 0,
  "vesting_balance": "0.000 STEEM",
  "reputation": -14004204351,
  "transfer_history": [],
  "market_history": [],
  "post_history": [],
  "vote_history": [],
  "other_history": [],
  "witness_votes": [],
  "tags_usage": [],
  "guest_bloggers": [],
  "rank": 874364
}

Withdraw Routes

IncomingOutgoing
Empty
Empty
{
  "incoming": [],
  "outgoing": []
}
From Date
To Date
steemdelegated 4.374 SP to @dvendetta
2026/05/17 23:45:36
delegateedvendetta
delegatorsteem
vesting shares7113.986986 VESTS
Transaction InfoBlock #106142859/Trx 98e71798ab2646d0e4798e192456ea9be23eb278
View Raw JSON Data
{
  "block": 106142859,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "7113.986986 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2026-05-17T23:45:36",
  "trx_id": "98e71798ab2646d0e4798e192456ea9be23eb278",
  "trx_in_block": 0,
  "virtual_op": 0
}
steemdelegated 2.706 SP to @dvendetta
2026/05/12 01:50:12
delegateedvendetta
delegatorsteem
vesting shares4401.776581 VESTS
Transaction InfoBlock #105973307/Trx 8791ac3587bbf3fe4767e837d685a9d8c49acb52
View Raw JSON Data
{
  "block": 105973307,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "4401.776581 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2026-05-12T01:50:12",
  "trx_id": "8791ac3587bbf3fe4767e837d685a9d8c49acb52",
  "trx_in_block": 0,
  "virtual_op": 0
}
steemdelegated 4.382 SP to @dvendetta
2026/04/25 23:07:18
delegateedvendetta
delegatorsteem
vesting shares7126.502742 VESTS
Transaction InfoBlock #105510524/Trx 12dc4c437629f77fe6ac24304c2a4d934534124d
View Raw JSON Data
{
  "block": 105510524,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "7126.502742 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2026-04-25T23:07:18",
  "trx_id": "12dc4c437629f77fe6ac24304c2a4d934534124d",
  "trx_in_block": 0,
  "virtual_op": 0
}
steemdelegated 2.732 SP to @dvendetta
2026/01/23 06:27:42
delegateedvendetta
delegatorsteem
vesting shares4443.323400 VESTS
Transaction InfoBlock #102850203/Trx 79abc89f9a3df2e2199d4580bfc8933b4274baf1
View Raw JSON Data
{
  "block": 102850203,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "4443.323400 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2026-01-23T06:27:42",
  "trx_id": "79abc89f9a3df2e2199d4580bfc8933b4274baf1",
  "trx_in_block": 3,
  "virtual_op": 0
}
steemdelegated 2.833 SP to @dvendetta
2024/12/17 01:47:15
delegateedvendetta
delegatorsteem
vesting shares4607.542597 VESTS
Transaction InfoBlock #91296623/Trx 57589d56460d253b7c155add3877392f9d4e9f66
View Raw JSON Data
{
  "block": 91296623,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "4607.542597 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2024-12-17T01:47:15",
  "trx_id": "57589d56460d253b7c155add3877392f9d4e9f66",
  "trx_in_block": 3,
  "virtual_op": 0
}
steemdelegated 2.937 SP to @dvendetta
2023/11/13 17:30:09
delegateedvendetta
delegatorsteem
vesting shares4776.676129 VESTS
Transaction InfoBlock #79850829/Trx 216f82a70d92f194b60a2790cbb855fe3c47f7d9
View Raw JSON Data
{
  "block": 79850829,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "4776.676129 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2023-11-13T17:30:09",
  "trx_id": "216f82a70d92f194b60a2790cbb855fe3c47f7d9",
  "trx_in_block": 4,
  "virtual_op": 0
}
steemdelegated 4.743 SP to @dvendetta
2023/09/21 21:14:30
delegateedvendetta
delegatorsteem
vesting shares7713.954915 VESTS
Transaction InfoBlock #78347123/Trx 533badacdb916cb818103e4144d74989775aecd0
View Raw JSON Data
{
  "block": 78347123,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "7713.954915 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2023-09-21T21:14:30",
  "trx_id": "533badacdb916cb818103e4144d74989775aecd0",
  "trx_in_block": 0,
  "virtual_op": 0
}
steemdelegated 4.879 SP to @dvendetta
2022/11/03 11:07:00
delegateedvendetta
delegatorsteem
vesting shares7935.636353 VESTS
Transaction InfoBlock #69112562/Trx 2199edf2f2fb3509a268b1ec6e8bbfbe4304f9e2
View Raw JSON Data
{
  "block": 69112562,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "7935.636353 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2022-11-03T11:07:00",
  "trx_id": "2199edf2f2fb3509a268b1ec6e8bbfbe4304f9e2",
  "trx_in_block": 1,
  "virtual_op": 0
}
steemdelegated 5.015 SP to @dvendetta
2022/01/17 10:25:48
delegateedvendetta
delegatorsteem
vesting shares8156.169584 VESTS
Transaction InfoBlock #60808784/Trx e260910be3491a843433b5d3bd9176b1c8c41142
View Raw JSON Data
{
  "block": 60808784,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "8156.169584 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2022-01-17T10:25:48",
  "trx_id": "e260910be3491a843433b5d3bd9176b1c8c41142",
  "trx_in_block": 2,
  "virtual_op": 0
}
steemdelegated 5.128 SP to @dvendetta
2021/06/14 00:22:21
delegateedvendetta
delegatorsteem
vesting shares8339.938242 VESTS
Transaction InfoBlock #54607198/Trx c35882a8f45f093bdb2194a5cce29d0ce2b60961
View Raw JSON Data
{
  "block": 54607198,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "8339.938242 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2021-06-14T00:22:21",
  "trx_id": "c35882a8f45f093bdb2194a5cce29d0ce2b60961",
  "trx_in_block": 1,
  "virtual_op": 0
}
steemdelegated 5.243 SP to @dvendetta
2020/12/11 10:42:09
delegateedvendetta
delegatorsteem
vesting shares8527.360216 VESTS
Transaction InfoBlock #49354683/Trx 0191d66611bb4363da3d5f1376ff27afd4db1ac9
View Raw JSON Data
{
  "block": 49354683,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "8527.360216 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2020-12-11T10:42:09",
  "trx_id": "0191d66611bb4363da3d5f1376ff27afd4db1ac9",
  "trx_in_block": 2,
  "virtual_op": 0
}
steemdelegated 1.176 SP to @dvendetta
2020/12/06 04:19:27
delegateedvendetta
delegatorsteem
vesting shares1912.543513 VESTS
Transaction InfoBlock #49206248/Trx a02ad27a576e32c6ea8ca6a4167789cbcb147145
View Raw JSON Data
{
  "block": 49206248,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "1912.543513 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2020-12-06T04:19:27",
  "trx_id": "a02ad27a576e32c6ea8ca6a4167789cbcb147145",
  "trx_in_block": 2,
  "virtual_op": 0
}
steemdelegated 5.247 SP to @dvendetta
2020/12/05 14:20:24
delegateedvendetta
delegatorsteem
vesting shares8533.568070 VESTS
Transaction InfoBlock #49189781/Trx dd06f4d292c9a0d82e8f2ee40bc392f115190207
View Raw JSON Data
{
  "block": 49189781,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "8533.568070 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2020-12-05T14:20:24",
  "trx_id": "dd06f4d292c9a0d82e8f2ee40bc392f115190207",
  "trx_in_block": 3,
  "virtual_op": 0
}
steemdelegated 1.181 SP to @dvendetta
2020/11/02 14:40:18
delegateedvendetta
delegatorsteem
vesting shares1920.017158 VESTS
Transaction InfoBlock #48256659/Trx e83cd883ef30e77fd0dea7a57a0ceeb876746c24
View Raw JSON Data
{
  "block": 48256659,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "1920.017158 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2020-11-02T14:40:18",
  "trx_id": "e83cd883ef30e77fd0dea7a57a0ceeb876746c24",
  "trx_in_block": 0,
  "virtual_op": 0
}
steemdelegated 5.371 SP to @dvendetta
2020/05/09 05:16:09
delegateedvendetta
delegatorsteem
vesting shares8736.373429 VESTS
Transaction InfoBlock #43216485/Trx ff49c4c4b08a38ac8258e4b6e8b859d5f3f05d43
View Raw JSON Data
{
  "block": 43216485,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "8736.373429 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2020-05-09T05:16:09",
  "trx_id": "ff49c4c4b08a38ac8258e4b6e8b859d5f3f05d43",
  "trx_in_block": 12,
  "virtual_op": 0
}
steemdelegated 1.201 SP to @dvendetta
2020/05/08 08:47:57
delegateedvendetta
delegatorsteem
vesting shares1953.311140 VESTS
Transaction InfoBlock #43192497/Trx 65c690bd7f61907a8a32241089b7cd1178f76974
View Raw JSON Data
{
  "block": 43192497,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "1953.311140 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2020-05-08T08:47:57",
  "trx_id": "65c690bd7f61907a8a32241089b7cd1178f76974",
  "trx_in_block": 8,
  "virtual_op": 0
}
steemdelegated 5.379 SP to @dvendetta
2020/04/15 21:19:39
delegateedvendetta
delegatorsteem
vesting shares8749.350848 VESTS
Transaction InfoBlock #42562223/Trx 2a9603ad95dc1c55d1bb6f23251353201cad3f4d
View Raw JSON Data
{
  "block": 42562223,
  "op": [
    "delegate_vesting_shares",
    {
      "delegatee": "dvendetta",
      "delegator": "steem",
      "vesting_shares": "8749.350848 VESTS"
    }
  ],
  "op_in_trx": 0,
  "timestamp": "2020-04-15T21:19:39",
  "trx_id": "2a9603ad95dc1c55d1bb6f23251353201cad3f4d",
  "trx_in_block": 13,
  "virtual_op": 0
}
2019/09/25 20:30:57
authorsteemitboard
bodyCongratulations @dvendetta! You received a personal award! <table><tr><td>https://steemitimages.com/70x70/http://steemitboard.com/@dvendetta/birthday2.png</td><td>Happy Birthday! - You are on the Steem blockchain for 2 years!</td></tr></table> <sub>_You can view [your badges on your Steem Board](https://steemitboard.com/@dvendetta) and compare to others on the [Steem Ranking](https://steemitboard.com/ranking/index.php?name=dvendetta)_</sub> **Do not miss the last post from @steemitboard:** <table><tr><td><a href="https://steemit.com/steemfest/@steemitboard/steemitboard-supports-the-steemfest-travel-reimbursement-fund"><img src="https://steemitimages.com/64x128/https://cdn.steemitimages.com/DQmXDHs9xfx8ZZ3DESFUqHRUQAcQT5kUWobArsRoJg2Yz1F/image.png"></a></td><td><a href="https://steemit.com/steemfest/@steemitboard/steemitboard-supports-the-steemfest-travel-reimbursement-fund">SteemitBoard supports the SteemFest⁴ Travel Reimbursement Fund.</a></td></tr></table> ###### [Vote for @Steemitboard as a witness](https://v2.steemconnect.com/sign/account-witness-vote?witness=steemitboard&approve=1) to get one more award and increased upvotes!
json metadata{"image":["https://steemitboard.com/img/notify.png"]}
parent authordvendetta
parent permlinkoverview-genetictransformation-of-plants-and-creation-of-transgenic-plants-ogm
permlinksteemitboard-notify-dvendetta-20190925t203057000z
title
Transaction InfoBlock #36739940/Trx c21aece6ecf931b6c1f8b728fcd2f9ac650d6c04
View Raw JSON Data
{
  "block": 36739940,
  "op": [
    "comment",
    {
      "author": "steemitboard",
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2019/05/12 14:34:27
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steemdelegated 5.622 SP to @dvendetta
2018/05/16 20:15:12
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steemdelegated 18.216 SP to @dvendetta
2018/02/21 23:06:12
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steemdelegated 18.342 SP to @dvendetta
2017/10/13 05:14:30
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2017/09/28 19:27:27
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2017/09/28 19:26:24
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2017/09/28 19:26:15
authorsteemcleaners
bodySource: https://books.google.co.uk/books?id=aSL-CAAAQBAJ&pg=PA109&lpg=PA109&dq=The+most+important+branch+of+in+vitro+culture+is+cloning,+also+called+micropropagation+or+vegetative+propagation.+And+the+aim+of+micropropagation+is+to+create+safely+possibilities+to+clone+higher+plants+disease-free,+faster+and+less+expensive+than+in+vivo&source=bl&ots=uzXw5sNAfd&sig=4DfZYKcmb9gE66Ne1zeBqxHUe2o&hl=en&sa=X&ved=0ahUKEwiq47WAzsjWAhWkKMAKHXxZA4oQ6AEIKTAA#v=onepage&q=The%20most%20important%20branch%20of%20in%20vitro%20culture%20is%20cloning%2C%20also%20called%20micropropagation%20or%20vegetative%20propagation.%20And%20the%20aim%20of%20micropropagation%20is%20to%20create%20safely%20possibilities%20to%20clone%20higher%20plants%20disease-free%2C%20faster%20and%20less%20expensive%20than%20in%20vivo&f=false Not indicating that the content you copy/paste is not your original work could be seen as [plagiarism. ](http://www.plagiarism.org/plagiarism-101/what-is-plagiarism/) Some tips to share content and add value: - Use a few sentences from your source in “quotes.” Use HTML tags or Markdown. - Linking to your source - Include your own original thoughts and ideas on what you have shared. Repeated plagiarized posts are considered spam. Spam is discouraged by the community, and may result in action from the [cheetah bot](https://steemit.com/steemitabuse/@cheetah/cheetah-bot-explained). Creative Commons: If you are posting content under a Creative Commons license, please attribute and link according to the specific license. If you are posting content under CC0 or Public Domain please consider noting that at the end of your post. If you are actually the original author, please do reply to let us know! Thank You!
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2017/09/28 19:25:57
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2017/09/28 19:24:54
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2017/09/28 19:24:51
authorsteemcleaners
bodySources: https://link.springer.com/chapter/10.1007/978-3-0348-8700-7_2 https://books.google.fr/books?id=1LWmOrVK940C&pg=PA579&lpg=PA579&dq=There+are+a+number+of+genetic+transformation+methods+developed+for+the+production+of+transgenic+plants.+Genetic+transformation+methods+in+plants+can+be+divided+mainly+into+two+classes-vector-mediated+gene+transfer+and+direct+gene+transfer+or+vector-less+gene+transfer.&source=bl&ots=0xcYlWRdW6&sig=yzQXS7UkV6yydnJ4vKKbJ6igEew&hl=en&sa=X&ved=0ahUKEwjMnIvQw8jWAhXFKcAKHWnPB1IQ6AEILjAB#v=onepage&q&f=false Not indicating that the content you copy/paste is not your original work could be seen as [plagiarism. ](http://www.plagiarism.org/plagiarism-101/what-is-plagiarism/) Some tips to share content and add value: - Use a few sentences from your source in “quotes.” Use HTML tags or Markdown. - Linking to your source - Include your own original thoughts and ideas on what you have shared. Repeated plagiarized posts are considered spam. Spam is discouraged by the community, and may result in action from the [cheetah bot](https://steemit.com/steemitabuse/@cheetah/cheetah-bot-explained). Creative Commons: If you are posting content under a Creative Commons license, please attribute and link according to the specific license. If you are posting content under CC0 or Public Domain please consider noting that at the end of your post. If you are actually the original author, please do reply to let us know! Thank You!
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2017/09/28 16:50:24
authorsuesa
bodySome sources for your info and pictures would be great, without them this post looks plagiarized (and pictures should always be credited).
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2017/09/28 15:38:12
authordvendetta
body![tech.jpg](https://steemitimages.com/DQmSuQDgqk7LdUWjypLGiMPiEdQ1U6u5mVCgTj9VKP59gy1/tech.jpg) Transformation genetics are based on the introduction of DNA into totipotent plant cells, followed by the regeneration of such cells into whole fertile plants. Transformation is a complex process and can occur by many different routes. Transformation genetics technology in plants raises issues of global importance, approached and resolved in very different ways, that often mix local, national and global perspectives. In India for example, attitudes to Genetic manipulation have been shaped in part by concerns about the influence of foreign multinationals, as opposed to home-grown technologies. India's Government supports local research into high-protein potatoes, high-yield mustard and drought- and salt-tolerant rice. But it has banned the import of maize or soya flour from US aid agencies, after several Indian environmental organisations protested against the genetic manipulation content of such products . In the US, there is a generally high level of acceptance and utilisation of GM foods and there is no requirement to label products derived from transgenic crops. Clearly, many factors outside science influence decision making, and these may well differ between countries. We will explore some of these issues, but initially, it is useful to have an overview of the position of GM crops globally. ![maps.jpg](https://steemitimages.com/DQmTqKgs5qx2qyBRu6a5gxVMSWq4sA44Xnk3F1xiWwev8pY/maps.jpg) ![tabl1.jpg](https://steemitimages.com/DQmabuAMHR4qZVnCY8UcATn67nnxppVJoUWMogr5zD6iEE5/tabl1.jpg) There are a number of genetic transformation methods developed for the production of transgenic plants. Genetic transformation methods in plants can be divided mainly into two classes—vector-mediated gene transfer and direct gene transfer or vector-less gene transfer. In this article we'll talk just about the Vector-Mediated or Indirect Gene Transfer, this method is appeared in 1970s with microbiologists Mary-Dell Chilton , Eugene W. Nester, and Milton P. Gordon, the elucidation of the mechanism of crown gall formation by _Agrobacterium tumefaciens_ .The discovery that virulent strains of _A. tumefaciens_ carried a large plasmid that conferred the ability to induce crown galls and that part of the plasmid (the T-DNA) was transferred to the plant genome of crown gall cells provided a natural gene transfer mechanism that could be exploited for plant transformation. ![cycl.jpg](https://steemitimages.com/DQmZEPGD8NCoTRJ8NKXtTjcusTZb3VFRZLUKSEK9oZ9Mxuw/cycl.jpg) The general strategy would therefore be to design a ‘recombinant’ plasmid containing the desired gene that codes for a desired trait that is to be transferred to the plant. The gene may be for resistance to herbicides, for example, or the ability, to synthesize a specific protein of commercial interest, such as an antibody or hormone. Next, the recombinant plasmid is transferred into the agrobacterium. Finally, the bacteria containing these modified Ti plasmids (without t-DNA) are inoculated into the host plant and these bacteria go about their business of inserting plasmid DNA fragments into the host plant genome. The first genetically engineered food now available in supermarkets, the ‘Flavor-Savr’ tomato, owes its existence to gene transfer by agrobacterium. Plant tissue such as terminal meristems as terminal meristems, or leaf discs, or cultured plant cells are co-cultivated or incubated with the a. tumefaciens having the recombinant plasmids, allowing the bacterium to infect the tissue or cells. The infected tissues are allowed to grow on shoot regeneration medium. During this time the transfer of genes into the plant genome takes place. ![stps.jpg](https://steemitimages.com/DQmQUV5krYmZEWUU4uFsXro1Fgzx5eANWqReMj1AyP1mDF6/stps.jpg) After transformation, cells are allowed to proliferate on selective medium to increase the amount of callus and kill nontransformed cells. Trans-genie plants can then be regenerated by two methods: somatic embryogenesis or organogenesis. Somatic embryogenesis involves the formation of embryogenic callus direct from somatic tissues. This recapitulates the entire developmental pathway, including the embryonic stage. Organogenesis involves the direct growth of shoots from the callus of transformed tissues or in some cases direct growth from transformed explants without a callus stage. The shoots can be transferred to rooting medium and regenerated into plants or grafted onto seedling rootstock and propagated. ![zate1.jpg](https://steemitimages.com/DQmPXXTQ3h8vUA9MrcudxaNGzmhjTMAHJ5HYU184VMGS2aG/zate1.jpg) In some species, only one regenerative process is possible under the conditions used for trans-formation.For example, transgenic rice and maize plants are generated pre-dominantly by somatic embryogenesis, and transgenic cassava plants can be generated only by the organogenesis of shoots. In other species, such as banana and soybean, both processes are possible and the method of choice depends on the starting material and culture conditions and which process produces transgenic plants the most rapidly and with the greatest efficiency. An alternative to these processes is the development of transgenic plants by true embryogenesis from transformed seeds, zygotes, or gametes that undergo diploidization. ![stg.jpg](https://steemitimages.com/DQmP1ubBHFcLRMVw35kAg8xJSCbFwKetGj48JLNfmNXCvVp/stg.jpg) The completely developed transgenic plants can be transferred to soil after proper acclimatization or hardening. The transgenic plants can be evaluated for the presence of the foreign gene and its proper expression can be analyzed by different sets of molecular techniques such as Southern hybridization, Northern hybridization, PCR, and also by enzyme assays. Once the transgenic plant is completely evaluated for its possible biological activities and its impact on environment and other ethical and safety issues, it can be recommended for release to farmers or companies. ![zat.jpg](https://steemitimages.com/DQmdQMmFz6XdASb2tPsWZUJ2qQc2NbJP3Kj7Y1ep2PHBmTi/zat.jpg) Genetically modified plants are now being commercialised in several countries as regulatory authorities consider that the balance of risk versus benefit is beneficial. However, numerous questions remain unanswered, especially the impact of these plants when used over large areas and under a range of variable environmental conditions. Some issues need to be re-evaluated [1,2]. Risk/safety analysis, as well as prospects of transgenic crops depend on the scale which is to be considered. Extrapolation of methods, and laboratory and greenhouse results, to large-scale farmers' fields, may provide useful preliminary data, but is not a sound approach to the study of the consequences of the commercial release of transgenic crops. Risk/safety analysis involves hazard identification and risk assessment. Hazards are scale-dependent and need to be tested on an appropriate scale. Change to a region's flora, for instance, is not a matter for a greenhouse test, but must be studied at the regional level. Risks associated with identified hazards depend on local conditions, e.g. non-proportionality of pollen spread with source size, regional variation of crop management practices, interaction between crops, genotype variability of populations of wild relatives, etc. A main concern is to estimate the value of predictability for agriculture and environment of results collected on different scales.
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      "body": "![tech.jpg](https://steemitimages.com/DQmSuQDgqk7LdUWjypLGiMPiEdQ1U6u5mVCgTj9VKP59gy1/tech.jpg)\n\n\nTransformation genetics  are based on the introduction of DNA into totipotent  plant cells, followed by the regeneration of such cells into whole fertile plants. Transformation is a complex process and can occur by many different routes.\n\n\nTransformation genetics    technology in plants raises issues of global importance, approached and resolved in very different ways, that often mix local, national and global perspectives. In India for example, attitudes to Genetic manipulation have been shaped in part by concerns about the influence of foreign multinationals, as   opposed to home-grown     technologies. India's Government supports local research into high-protein potatoes, high-yield  mustard and drought- and salt-tolerant rice. But it has banned the import of maize or soya flour from US aid agencies, after several Indian environmental organisations protested against   the genetic  manipulation  content  of such products . In the US, there  is  a generally  high  level  of  acceptance  and utilisation of GM foods and there is no requirement to label products derived from transgenic crops. Clearly, many factors outside science influence decision making, and these may well differ between countries. We will explore some of these issues, but initially, it is useful to have an overview of the position of GM crops globally.\n\n\n\n\n\n\n\n\n\n\n\n\n![maps.jpg](https://steemitimages.com/DQmTqKgs5qx2qyBRu6a5gxVMSWq4sA44Xnk3F1xiWwev8pY/maps.jpg)\n\n\n![tabl1.jpg](https://steemitimages.com/DQmabuAMHR4qZVnCY8UcATn67nnxppVJoUWMogr5zD6iEE5/tabl1.jpg)\n\n\n\nThere are a number of genetic transformation methods developed for the production of transgenic plants. Genetic transformation methods in plants can be divided mainly into two classes—vector-mediated gene transfer and direct gene transfer or vector-less gene transfer. \n\n\n\nIn this article we'll  talk  just about the Vector-Mediated or Indirect Gene Transfer, this method is appeared in 1970s with  microbiologists Mary-Dell Chilton , Eugene W. Nester, and Milton P. Gordon, the elucidation of the mechanism of crown gall formation by _Agrobacterium tumefaciens_ .The discovery that virulent strains of _A. tumefaciens_ carried a large plasmid that conferred the ability to induce crown galls and that part of the plasmid (the T-DNA) was transferred to the plant genome of crown gall cells provided a natural gene transfer mechanism that could be exploited for plant transformation.\n\n\n![cycl.jpg](https://steemitimages.com/DQmZEPGD8NCoTRJ8NKXtTjcusTZb3VFRZLUKSEK9oZ9Mxuw/cycl.jpg)\n\n\n\nThe general strategy would therefore be to design a ‘recombinant’ plasmid containing the desired gene that codes for a desired trait that is to be transferred to the plant. The gene may be for resistance to herbicides, for example, or the ability, to synthesize a specific protein of commercial interest, such as an antibody or hormone. Next, the recombinant plasmid is transferred into the agrobacterium. Finally, the bacteria containing these modified Ti plasmids (without t-DNA) are inoculated into the host plant and these bacteria go about their business of inserting plasmid DNA fragments into the host plant genome. The first genetically engineered food now available in supermarkets, the ‘Flavor-Savr’ tomato, owes its existence to gene transfer by agrobacterium. Plant tissue such as terminal meristems as terminal meristems, or leaf discs, or cultured plant cells are co-cultivated or incubated with the a. tumefaciens having the recombinant plasmids, allowing the bacterium to infect the tissue or cells. The infected tissues are allowed to grow on shoot regeneration medium. During this time the transfer of genes into the plant genome takes place.\n\n![stps.jpg](https://steemitimages.com/DQmQUV5krYmZEWUU4uFsXro1Fgzx5eANWqReMj1AyP1mDF6/stps.jpg)\n\nAfter transformation, cells are allowed to proliferate on selective medium to increase the amount of callus and kill nontransformed cells. Trans-genie plants can then be regenerated by two methods: somatic embryogenesis or organogenesis. Somatic embryogenesis involves the formation of embryogenic callus direct from somatic tissues. This recapitulates the entire developmental pathway, including the embryonic stage. Organogenesis involves the direct growth of shoots from the callus of transformed tissues or in some cases direct growth from transformed explants without a callus stage. The shoots can be transferred to rooting medium and regenerated into plants or grafted onto seedling rootstock and propagated.\n\n![zate1.jpg](https://steemitimages.com/DQmPXXTQ3h8vUA9MrcudxaNGzmhjTMAHJ5HYU184VMGS2aG/zate1.jpg)\n\nIn some species, only one regenerative process is possible under the conditions used for trans-formation.For example, transgenic rice and maize plants are generated pre-dominantly by somatic embryogenesis, and transgenic cassava plants can be generated only by the organogenesis of shoots. In other species, such as banana and soybean, both processes are possible and the method of choice depends on the starting material and culture conditions and which process produces transgenic plants the most rapidly and with the greatest efficiency. An alternative to these processes is the development of transgenic plants by true embryogenesis from transformed seeds, zygotes, or gametes that undergo diploidization. \n\n![stg.jpg](https://steemitimages.com/DQmP1ubBHFcLRMVw35kAg8xJSCbFwKetGj48JLNfmNXCvVp/stg.jpg)\n\nThe completely developed transgenic plants can be transferred to soil after proper acclimatization or hardening. The transgenic plants can be evaluated for the presence of the foreign gene and its proper expression can be analyzed by different sets of molecular techniques such as Southern hybridization, Northern hybridization, PCR, and also by enzyme assays. Once the transgenic plant is completely evaluated for its possible biological activities and its impact on environment and other ethical and safety issues, it can be recommended for release to farmers or companies.\n![zat.jpg](https://steemitimages.com/DQmdQMmFz6XdASb2tPsWZUJ2qQc2NbJP3Kj7Y1ep2PHBmTi/zat.jpg)\n\n\nGenetically modified plants are now being commercialised in several countries as regulatory authorities consider that the balance of risk versus benefit is beneficial. However, numerous questions remain unanswered, especially the impact of these plants when used over large areas and under a range of variable environmental conditions. Some issues need to be re-evaluated [1,2]. Risk/safety analysis, as well as prospects of transgenic crops depend on the scale which is to be considered. Extrapolation of methods, and laboratory and greenhouse results, to large-scale farmers' fields, may provide useful preliminary data, but is not a sound approach to the study of the consequences of the commercial release of transgenic crops. Risk/safety analysis involves hazard identification and risk assessment. Hazards are scale-dependent and need to be tested on an appropriate scale. Change to a region's flora, for instance, is not a matter for a greenhouse test, but must be studied at the regional level. Risks associated with identified hazards depend on local conditions, e.g. non-proportionality of pollen spread with source size, regional variation of crop management practices, interaction between crops, genotype variability of populations of wild relatives, etc. A main concern is to estimate the value of predictability for agriculture and environment of results  collected  on different scales.",
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2017/09/26 23:04:42
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2017/09/26 23:04:33
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2017/09/26 23:03:21
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2017/09/26 12:13:27
authordvendetta
permlinkthe-plants-cell-and-tissus-culture-the-futur-of-the-agrecultur
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2017/09/26 12:10:36
authordvendetta
body![man.jpg](https://steemitimages.com/DQmQ8fePoxv53AMjRkK1cEWU1th2VETcEVrrH5NsFzcniGg/man.jpg) Many girls prefer a certain type of man, not necessarilly the most handsome, often without knowing why, if a girl is shown phtographs of men who are very different, but all acceptable, she will pick out serveral who seem especially attractive to her. Another girl may see nothing interesting in them at all. One would have to delve into the buried memories of childhood to explain these selective attraction.
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title__Attract womens, it's out of society rules__
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      "body": "![man.jpg](https://steemitimages.com/DQmQ8fePoxv53AMjRkK1cEWU1th2VETcEVrrH5NsFzcniGg/man.jpg)\n\n\nMany girls prefer a certain type of man, not necessarilly the most handsome, often without knowing why, if a girl is shown phtographs of men who are very different, but all acceptable, she will pick out serveral who seem especially attractive to her.\n\nAnother girl may see nothing interesting in them at all. One would have to delve into the buried memories of childhood to explain these selective attraction.",
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2017/09/26 11:23:03
authordvendetta
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2017/09/26 11:22:36
authordvendetta
body<><> ![fleur.jpg](https://steemitimages.com/DQmV4MkhzMP5XTFvi5pfAPPh3HqMc4ZeV8r3TgNn3yuzE1e/fleur.jpg)<> <> __In vitro culture__ of plants is defined as the culture on nutrient media under __sterile conditions__ of plants, embryos, organs, explants, tissues, cells and protoplasts. The most important branch of in vitro culture is __cloning__, also called __micropropagation__ or __vegetative propagation.__ And the aim of micropropagation is to create safely possibilities to clone higher plants disease-free, __faster and less expensive than in vivo.__ ![steps.jpg](https://steemitimages.com/DQmc6SjR9YsKNdTAMGJXmGGLehoarAvu9iRSh2YxMxmxc5f/steps.jpg) schematics steps of in vitro culture of potatoes In vitro cloning also offers possibilities to clone plants in cases where it is impossible in vivo. The advantage of this technology is that is enables the production of __disease--free plants__ and thereby also __facilitates the so-called phytosanitary transport.__ ![nnnnn.jpg](https://steemitimages.com/DQmVREGqemo2P223KBAccsDUpzXNYitRwT57fDi2H8jiXj3/nnnnn.jpg) In addition, the multiplication of plants by __tissue culture - micropropagation__, offers many advantages over conventional methods for __the multiplication of large numbers of plants__ __independent of climatic conditions__ and with __conservation of space and time__. Furthermore in vitro derivea plants are frequently more vigorous and of superior quality, often justifying the term "elite" plants in comparison to those produced by in vivo methods. ![tow.jpg](https://steemitimages.com/DQmTTrrGPYKEgS3iUUmMik1c3FNxG5kZqebMHGwZQePeNtU/tow.jpg) The multiplication of plants by __tissue cultures__ centres around the formation and multiplication of shoot meristems. Two main pathways are involved, one is the regeneration of plants from existing meristems - axillary and apical meristems which results in the production of clonally stable plantlets. The other is by the induction of de novo meristems, adventitious meristems and somatic embryos in cultured organs/tissues/ callus. ![calus.jpg](https://steemitimages.com/DQma9BynsyVTc7zBuN1P9TKgeWmgw4pcLBbFfTf5SA9q67b/calus.jpg) Whilst this de novo pathway is much more productive it often results in progenys which are not true to type and in the production of somaclonal variants, this phenomenon is, however, being exploited in the continual search for new improved plant varieties. The transfer of in vitro-cultured plantlets to in vivo conditions is one of the most critical stages of the micropropagation process. Tody __plant tissue culture technology__ has introduced a new phase into plant multiplication and is being increasingly utilized in plant breeding, and it became 21st century agriculture, mor than that __plant tissue culture technology__ it's one of the important keys of science that can make the human being able to colonize the moon. ![mars.jpg](https://steemitimages.com/DQmTtiG2u7B4i9iqCxh565eVf4bucgf5G7KdUCRYokA2eJQ/mars.jpg)
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permlinkthe-plants-cell-and-tissus-culture-the-futur-of-the-agrecultur
titleThe Plants Cell and Tissus Culture #The futur of The agrecultur
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      "body": "<><>  ![fleur.jpg](https://steemitimages.com/DQmV4MkhzMP5XTFvi5pfAPPh3HqMc4ZeV8r3TgNn3yuzE1e/fleur.jpg)<> <> \n\n\n__In vitro culture__ of  plants  is defined as the culture on nutrient media under __sterile conditions__ of plants, embryos, organs, explants, tissues, cells and protoplasts. \n\nThe most important branch of in vitro culture is __cloning__, also called __micropropagation__ or __vegetative propagation.__  And the aim of micropropagation is to create safely possibilities to clone higher plants disease-free, __faster and less expensive than in vivo.__\n\n\n\n\n![steps.jpg](https://steemitimages.com/DQmc6SjR9YsKNdTAMGJXmGGLehoarAvu9iRSh2YxMxmxc5f/steps.jpg)\nschematics steps of in vitro culture of potatoes\n\n\n\n\n\n\nIn vitro cloning also offers possibilities to clone plants in cases where it is impossible in vivo. The advantage of this technology is that is enables the production of __disease--free plants__  and thereby also __facilitates the so-called phytosanitary transport.__\n\n![nnnnn.jpg](https://steemitimages.com/DQmVREGqemo2P223KBAccsDUpzXNYitRwT57fDi2H8jiXj3/nnnnn.jpg)\n\nIn addition, the multiplication of plants by __tissue culture - micropropagation__, offers many advantages over conventional methods for __the multiplication of large numbers of plants__  __independent of climatic conditions__ and with __conservation of space and time__.\n\n\n\n\n\n\n\n\nFurthermore in vitro derivea plants are frequently more vigorous and of superior quality, often justifying the term \"elite\" plants in comparison to those produced by in vivo methods.\n\n![tow.jpg](https://steemitimages.com/DQmTTrrGPYKEgS3iUUmMik1c3FNxG5kZqebMHGwZQePeNtU/tow.jpg)\n\n\n\nThe multiplication of plants by __tissue cultures__ centres around the formation and multiplication of shoot meristems.\nTwo main pathways are involved, one is the regeneration of plants from existing meristems - axillary and apical meristems which results in the production of clonally stable plantlets.\n\nThe other is by the induction of de novo meristems, adventitious meristems and somatic embryos in cultured organs/tissues/ callus. \n\n![calus.jpg](https://steemitimages.com/DQma9BynsyVTc7zBuN1P9TKgeWmgw4pcLBbFfTf5SA9q67b/calus.jpg)\n\n\nWhilst this de novo pathway is much more productive it often results in progenys which are not true to type and in the production of somaclonal variants, this phenomenon is, however, being exploited in the continual search for new improved plant varieties.\n\nThe transfer of in vitro-cultured plantlets to in vivo conditions is one of the most critical stages of the micropropagation process.\n\nTody __plant tissue culture technology__ has introduced a new phase into plant multiplication and is being increasingly utilized in plant breeding, and it became 21st century agriculture, mor than that __plant tissue culture technology__  it's  one of the important keys of science that can make the human being able to colonize the moon.\n\n\n\n![mars.jpg](https://steemitimages.com/DQmTtiG2u7B4i9iqCxh565eVf4bucgf5G7KdUCRYokA2eJQ/mars.jpg)",
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2017/09/25 19:49:57
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2017/09/25 19:25:36
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