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Merck
CN

F3290

Millipore

FLAG® Peptide

≥85% (HPLC), lyophilized powder

别名:

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

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About This Item

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

产品名称

FLAG® 肽, lyophilized powder

方案

≥85% (HPLC)

质量水平

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

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® M1M2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。

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

从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

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访问文档库

Omar H Vandal et al.
Nature medicine, 14(8), 849-854 (2008-07-22)
Acidification of the phagosome is considered to be a major mechanism used by macrophages against bacteria, including Mycobacterium tuberculosis (Mtb). Mtb blocks phagosome acidification, but interferon-gamma (IFN-gamma) restores acidification and confers antimycobacterial activity. Nonetheless, it remains unclear whether acid kills
Barbara G Mellone et al.
PLoS genetics, 7(5), e1002068-e1002068 (2011-05-19)
Semi-conservative segregation of nucleosomes to sister chromatids during DNA replication creates gaps that must be filled by new nucleosome assembly. We analyzed the cell-cycle timing of centromeric chromatin assembly in Drosophila, which contains the H3 variant CID (CENP-A in humans)
Jingxiang Huang et al.
Cancer research, 69(15), 6107-6114 (2009-07-16)
Mutations in the TSC1 and TSC2 tumor suppressor genes give rise to the neoplastic disorders tuberous sclerosis complex (TSC) and lymphangioleiomyomatosis. Their gene products form a complex that is a critical negative regulator of mammalian target of rapamycin (mTOR) complex
Zheng Xu et al.
Molecular cell, 35(4), 426-441 (2009-09-01)
Accurate chromosome segregation during mitosis and meiosis depends on shugoshin proteins that prevent precocious dissociation of cohesin from centromeres. Shugoshins associate with PP2A, which is thought to dephosphorylate cohesin and thereby prevent cleavage by separase during meiosis I. A crystal
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

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