跳转至内容
Merck
所有图片(1)

Key Documents

View All Documentation

F3290

Millipore

FLAG® Peptide

≥85% (HPLC), lyophilized powder

别名:

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

登录查看公司和协议定价
所有图片(1)

About This Item

经验公式（希尔记法）:
C41H60N10O20
分子量:
1012.97
MDL號碼:
MFCD02262135
分類程式碼代碼:
12352202
PubChem物質ID:
329799698
NACRES:
NA.32

product name

FLAG® 肽, lyophilized powder

化驗

≥85% (HPLC)

品質等級

200

形狀

lyophilized powder

分子量

1012.97 Da

運輸包裝

wet ice

儲存溫度

2-8°C

SMILES 字串

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 密鑰

XZWYTXMRWQJBGX-VXBMVYAYSA-N

相关类别

一般說明

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。

應用

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。

準備報告

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。

其他說明

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)

法律資訊

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ （Lot或Batch）字后找到。

已有该产品？

在文件库中查找您最近购买产品的文档。

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)
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
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)
查看所有相关文献

相关内容

Protein Purification

Protein purification techniques, reagents, and protocols for purifying recombinant proteins using methods including, ion-exchange, size-exclusion, and protein affinity chromatography.

Protein Purification

Protein purification techniques, reagents, and protocols for purifying recombinant proteins using methods including, ion-exchange, size-exclusion, and protein affinity chromatography.

Protein Expression

Protein expression technologies for expressing recombinant proteins in E. coli, insect, yeast, and mammalian expression systems for fundamental research and the support of therapeutics and vaccine production.

Protein Expression

Protein expression technologies for expressing recombinant proteins in E. coli, insect, yeast, and mammalian expression systems for fundamental research and the support of therapeutics and vaccine production.

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门