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Merck
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주요 문서

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16-156

Millipore

Protein A Agarose, Fast Flow

Protein A Agarose, Fast Flow suitable for medium and low-pressure chromatography, immunoprecipitation and antibody purification.

동의어(들):

Protein A resin

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모든 사진(1)

About This Item

UNSPSC 코드:
41116133
eCl@ss:
32160801
NACRES:
NA.56
가격 및 재고 정보를 현재 이용할 수 없음 고객지원팀으로 연락바랍니다.

양식

liquid

제조업체/상표

Upstate®

기술

affinity chromatography: suitable
immunoprecipitation (IP): suitable
western blot: suitable

배송 상태

wet ice

일반 설명

Protein A is an immunoglobulin (Ig)-binding protein used to purify large amounts of IgG.[1] It binds to the Fc part of the antibody at the CH2–CH3 interface.[2] Protein A-agarose might be suitable for low-pressure antibody isolation.[1]
Recombinant Protein A covalently coupled to highly cross-linked 6% agarose beads.

Binding capacity: 40mg human IgG/ml agarose

애플리케이션

Protein A Agarose, Fast Flow has been used in immunoprecipitation[3][4] and chromatin immunoprecipitation (ChIP).[5]

품질

routinely evaluated in immunoprecipitation

물리적 형태

sterile distilled water containing 0.01% thimerosal

법적 정보

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

면책조항

For U.S. Customers: Contains mercury; Do not place in trash - dispose according to local, state, or federal laws.

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

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문서 라이브러리 방문

Lei Jiang et al.
Investigative ophthalmology & visual science, 61(5), 41-41 (2020-05-24)
To identify the pathogenic gene of infantile nystagmus syndrome (INS) in three Chinese families and explore the potential pathogenic mechanism of FERM domain-containing 7 (FRMD7) mutations. Genetic testing was performed via Sanger sequencing. Western blotting was used to analyze protein
Simon Schenk et al.
American journal of physiology. Endocrinology and metabolism, 291(2), E254-E260 (2006-05-04)
Although the increase in fatty acid oxidation after endurance exercise training has been linked with improvements in insulin sensitivity and overall metabolic health, the mechanisms responsible for increasing fatty acid oxidation after exercise training are not completely understood. The primary
Ghia M Euskirchen et al.
Genome research, 17(6), 898-909 (2007-06-15)
Recent progress in mapping transcription factor (TF) binding regions can largely be credited to chromatin immunoprecipitation (ChIP) technologies. We compared strategies for mapping TF binding regions in mammalian cells using two different ChIP schemes: ChIP with DNA microarray analysis (ChIP-chip)
Chih-Chin Huang et al.
The Journal of biological chemistry, 284(25), 17206-17215 (2009-04-15)
G protein-coupled receptor (GPCR) kinases (GRKs) phosphorylate activated GPCRs and initiate their desensitization. Many prior studies suggest that activated GPCRs dock to an allosteric site on the GRKs and thereby stimulate kinase activity. The extreme N-terminal region of GRKs is
Yong Cheng et al.
Nature, 515(7527), 371-375 (2014-11-21)
To broaden our understanding of the evolution of gene regulation mechanisms, we generated occupancy profiles for 34 orthologous transcription factors (TFs) in human-mouse erythroid progenitor, lymphoblast and embryonic stem-cell lines. By combining the genome-wide transcription factor occupancy repertoires, associated epigenetic
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