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Merck
CN

A4596

Millipore

ANTI-FLAG® M1琼脂糖亲和凝胶

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别名:
抗-ddddk, 抗-dykddddk
UNSPSC代码:
12352203
NACRES:
NA.32

偶联物

agarose conjugate

质量水平

抗体产品类型

primary antibodies

形式

suspension

同位素/亚型

IgG12b

容量

≥0.6 mg/mL, gel binding capacity

储存温度

−20°C

一般描述

ANTI-FLAG®M1琼脂亲和凝胶是一种纯化小鼠IgG2B单克隆抗体共价连接到琼脂糖上。

特异性

结合特异性:FLAG 序列
N-Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys-C自由N末端

应用

用于纯化N末端FLAG融合蛋白。由于结合过程不依赖Ca2+,蛋白质能采用含EDTA的缓冲液洗脱,也可以使用FLAG多肽或甘油-HLC缓冲液(pH3)通过标准方法洗脱。ANTI-FLAG M1不会和Met-FLAG融合蛋白结合,所以这种树脂不适合纯化未加工处理的细胞质表达融合蛋白。

该亲和凝胶可用于N末端FLAG融合蛋白的钙介导纯化。

免疫沉淀(IP):适用

洗脱方法:FLAG多肽、甘氨酸、pH3.5 EDTA

更多产品信息请访问我们的FLAG®应用页面。

特点和优势

  • 通常从粗裂解物中纯化融合蛋白,然后只使用一步层析,纯化成单条带
  • 用EDTA温和洗脱,将融合蛋白从亲和树脂上洗脱下来。
  • FLAG多肽溶液可以用于FLAG融合蛋白温和地,非变性洗脱。

外形

球形琼脂糖悬浮在含10 mM磷酸钠、150mM NaCl (pH7.4)、0.02% (w/v) 叠氮化钠的50%甘油溶液中

其他说明

ANTI-FLAG® M1并不会和Met-FLAG融合蛋白结合,所以这种树脂不适合纯化未处理的细胞质表达融合蛋白。

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

相关产品

产品编号
说明
价格

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

常规特殊物品

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

  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. Will Product A4596, ANTI-FLAG® M1 Agarose Affinity Gel, work for my C-terminal FLAG-tagged protein?

    No.  The M1 FLAG antibody resin will only bind proteins that are free N-terminal FLAG tagged proteins.  It will not recognize C-terminal FLAG tagged proteins or Met-N-terminal FLAG tagged proteins.

  4. Can I use Phosphate Buffered Saline (PBS) instead of Tris Buffered Saline (TBS) with Product A4596, ANTI-FLAG® M1 Agarose Affinity Gel?

    We do not recommend the use of phosphate buffers since calcium is required for binding.  This can result in the formation of insoluble calcium phosphates in the presence of PBS.

  5. How much calcium is required for binding of my FLAG-tagged protein to Product A4596, ANTI-FLAG® M1 Agarose Affinity Gel?

    10 mM calcium chloride is recommended for binding.

  6. What reagents are compatible with Product A4596, ANTI-FLAG® M1 Agarose Affinity Gel?

    The ANTI-FLAG M1 Affinity Gel is resistant to the following detergents: 5.0 % Tween-20; 5.0 % Triton X-100; 0.1 % NP-40; 0.1 % CHAPS and 0.2 % digitonin. It can also be used with 1.0 M NaCl or 1.0 M urea. Do not use the gel in the presence of SDS, deoxycholate or guanidine HCl.

  7. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  8. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  9. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

Ai Lu et al.
Biochemical and biophysical research communications, 513(3), 746-752 (2019-04-17)
Phosphoribosylformylglycinamidine synthase (PFAS) is an essential enzyme in de novo synthesis of purine. Previously, PFAS has been reported to modulate RIG-I activation during viral infection via deamidation. In this study, we sought to identify potential substrates that PFAS can deamidate.
Fenju Lai et al.
Chinese journal of cancer, 31(9), 440-448 (2012-08-03)
A recently identified protein, FAN1 (FANCD2-associated nuclease 1, previously known as KIAA1018), is a novel nuclease associated with monoubiquitinated FANCD2 that is required for cellular resistance against DNA interstrand crosslinking (ICL) agents. The mechanisms of FAN1 regulation have not yet
Bo Zhou et al.
Journal of molecular endocrinology, 55(3), 231-243 (2015-09-17)
Progranulin (PGRN) has recently emerged as an important regulator for insulin resistance. However, the direct effect of PGRN in vivo and the underlying role of progranulin in adipose insulin resistance involving the autophagy mechanism is not fully understood. In this
E Di Zazzo et al.
TheScientificWorldJournal, 2014, 565839-565839 (2014-08-13)
Recent studies have shown that hyperinsulinemia may increase the cancer risk. Moreover, many tumors demonstrate an increased activation of IR signaling pathways. Phosphatidylinositol 3-kinase (PI3K) is necessary for insulin action. In epithelial cells, which do not express GLUT4 and gluconeogenic
Elayanambi Sundaramoorthy et al.
Molecular cell, 65(4), 751-760 (2017-01-31)
Ribosomes that experience terminal stalls during translation are resolved by ribosome-associated quality control (QC) pathways that oversee mRNA and nascent chain destruction and recycle ribosomal subunits. The proximal factors that sense stalled ribosomes and initiate mammalian ribosome-associated QC events remain

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