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Merck
CN

F3290

FLAG® 肽

≥85% (HPLC), lyophilized powder

别名:

Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys, ddddk肽, dykddddk肽

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关于此项目

经验公式（希尔记法）:
C41H60N10O20
分子量:
1012.97
MDL编号:
MFCD02262135
UNSPSC代码:
12352202
PubChem化学物质编号:
329799698
NACRES:
NA.32

主要文件

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产品名称

FLAG® 肽, lyophilized powder

方案

≥85% (HPLC)

质量水平

200

表单

lyophilized powder

分子量

1012.97 Da

运输

wet ice

储存温度

2-8°C

SMILES字符串

NCCCC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](N)CC(O)=O)C(O)=O

InChI

1S/C41H60N10O20/c42-11-3-1-5-22(45-36(65)24(13-19-7-9-20(52)10-8-19)47-34(63)21(44)14-29(53)54)35(64)48-26(16-31(57)58)38(67)50-28(18-33(61)62)40(69)51-27(17-32(59)60)39(68)49-25(15-30(55)56)37(66)46-23(41(70)71)6-2-4-12-43/h7-10,21-28,52H,1-6,11-18,42-44H2,(H,45,65)(H,46,66)(H,47,63)(H,48,64)(H,49,68)(H,50,67)(H,51,69)(H,53,54)(H,55,56)(H,57,58)(H,59,60)(H,61,62)(H,70,71)/t21-,22-,23-,24-,25-,26-,27-,28-/m0/s1

InChI key

XZWYTXMRWQJBGX-VXBMVYAYSA-N

相关类别

一般描述

FLAG肽用于从抗-FLAG M1或抗-FLAG M2抗体（在溶液中或与琼脂糖凝胶结合）的氨基末端、Met-氨基末端或羧基末端FLAG融合蛋白的竞争性洗脱。

应用

温和的将FLAG融合蛋白从抗-FLAG® M1 和 M2亲和树脂上洗脱。通常的工作浓度是100 μg/ml。将不会洗脱3X FLAG融合蛋白。对于该应用，使用3X FLAG肽F4799。

请访问我们的FLAG®应用门户网站，了解更多产品详情。

制备说明

如需储备溶液，可溶解于TBS（10mM Tris HCL, 150 mM NaCl, pH7.4）至5 mg/mL的终浓度。

其他说明

2024年CiteAb奖——成功的帕金森研究供应商(2024 CiteAb Award Winner for Supplier Succeeding in Parkinson′s Research)

法律信息

ANTI-FLAG is a registered trademark of Merck KGaA, Darmstadt, Germany
FLAG is a registered trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

常规特殊物品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000498057
0000498057
0000460908
0000460909
0000348007

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Tong Zhou et al.
Nucleic acids research, 33(1), 289-297 (2005-01-14)
Tyrosyl-DNA phosphodiesterase (TDP1) is a DNA repair enzyme that removes peptide fragments linked through tyrosine to the 3' end of DNA, and can also remove 3'-phosphoglycolates (PGs) formed by free radical-mediated DNA cleavage. To assess whether TDP1 is primarily responsible
Kenjiro Hanaoka et al.
Magnetic resonance imaging, 26(5), 608-617 (2008-02-01)
Simple low molecular weight (MW) chelates of Gd(3+) such as those currently used in clinical MRI are considered too insensitive for most molecular imaging applications. Here, we evaluated the detection limit (DL) of a molecularly targeted low MW Gd(3+)-based T(1)
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Cancer research, 69(15), 6107-6114 (2009-07-16)
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PLoS genetics, 7(5), e1002068-e1002068 (2011-05-19)
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