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Merck
CN

P6649

Protein A–Sepharose 6MB

aqueous ethanol suspension

别名:

Protein A–Agarose macrobeads

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关于此项目

UNSPSC Code:
41106500
NACRES:
NA.56
MDL number:
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产品名称

Protein A–Sepharose 6MB, aqueous ethanol suspension

form

aqueous ethanol suspension

extent of labeling

~1 mg per mL

matrix activation

cyanogen bromide

matrix attachment

amino

matrix spacer

1 atom

capacity

~6 mg/mL binding capacity (human IgG)

storage temp.

2-8°C

Quality Level

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Application

Protein A-Sepharose is used for affinity chromatography, antibody purification and characterization, immunoaffinity matrices, protein chromatography, protein A, G and L resins, and recombinant protein expression and analysis. Protein A-Sepharose has been used to develop strategies for investigating protein interactions, to improve the detection of celiac disease, and to study diabetes in children.
Protein A–Sepharose 6MB has been used in immunoprecipitation.

General description

P6649-10ml′s updated product number is GE17-0469-01

Physical form

Suspension in 20% ethanol

Legal Information

Sepharose is a trademark of Cytiva

pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

100.4 °F

flash_point_c

38 °C

法规信息

常规特殊物品
危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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G V Hillyer et al.
The American journal of tropical medicine and hygiene, 38(3), 547-552 (1988-05-01)
Total RNA containing messenger RNA has been isolated from adult Fasciola hepatica and translated in vitro using the rabbit reticulocyte lysate system. L-[35S]-methionine labeled translation products have been immunoprecipitated with sera collected from rabbits infected with F. hepatica, rabbits immunized
L F Wang et al.
Gene, 169(1), 53-58 (1996-02-22)
Epitope tagging (Eta) is becoming an increasingly useful technique in molecular biology and biotechnology for the detection, characterisation and purification of recombinant proteins (re-proteins). Here we describe a novel Eta system composed of two different monoclonal antibodies (mAb; D11 and
Nikolai Peschek et al.
The EMBO journal, 38(16), e101650-e101650 (2019-07-18)
Small regulatory RNAs (sRNAs) are crucial components of many stress response systems. The envelope stress response (ESR) of Gram-negative bacteria is a paradigm for sRNA-mediated stress management and involves, among other factors, the alternative sigma factor E (σE ) and
Gaurav Dugar et al.
Molecular cell, 69(5), 893-905 (2018-03-03)
Cas9 nucleases naturally utilize CRISPR RNAs (crRNAs) to silence foreign double-stranded DNA. While recent work has shown that some Cas9 nucleases can also target RNA, RNA recognition has required nuclease modifications or accessory factors. Here, we show that the Campylobacter
Nikolai Peschek et al.
The EMBO journal, 38(16), e101650-e101650 (2019-07-18)
Small regulatory RNAs (sRNAs) are crucial components of many stress response systems. The envelope stress response (ESR) of Gram-negative bacteria is a paradigm for sRNA-mediated stress management and involves, among other factors, the alternative sigma factor E (σE ) and

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