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Merck
모든 사진(1)

문서

04-047

Sigma-Aldrich

Anti-CUGBP2 Antibody, clone 1H2

clone 1H2, Upstate®, from mouse

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About This Item

UNSPSC 코드:
12352203
eCl@ss:
32160702
NACRES:
NA.41

생물학적 소스

mouse

Quality Level

항체 형태

purified immunoglobulin

항체 생산 유형

primary antibodies

클론

1H2, monoclonal

종 반응성

human

제조업체/상표

Upstate®

기술

western blot: suitable

동형

IgG1

UniProt 수납 번호

배송 상태

dry ice

타겟 번역 후 변형

unmodified

유전자 정보

human ... CELF2(10659)

특이성

CuGBP2

면역원

A synthetic peptide corresponding to amino acids 209-415 of human CuGBP2.

애플리케이션

Research Category
Protein Trafficking
Research Sub Category
RNA Metabolism & Binding Proteins

RNA Binding Protein (RBP)
This Anti-CUGBP2 Antibody, clone 1H2 is validated for use in WB for the detection of CUGBP2.

품질

Routinely evaluated by immunoblot.

표적 설명

56 kDa

물리적 형태

100 μg of Protein A purified mouse monoclonal IgG1 in 100μl of 1X PBS, pH 7.0, 0.1% Azide.
Format: Purified
Protein A purified

저장 및 안정성

2 years at -20°C from date of shipment

법적 정보

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

면책조항

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리 방문

Debnath Mukhopadhyay et al.
Annals of the New York Academy of Sciences, 1010, 504-509 (2004-03-23)
Posttranscriptional control of gene expression plays a key role in regulating gene expression in cells undergoing apoptosis. Cyclooxygenase-2 (COX-2) is a crucial enzyme in the conversion of arachidonic acid to prostaglandin E2 (PGE(2)) and is significantly upregulated in many types
P Lichtner et al.
Journal of molecular medicine (Berlin, Germany), 80(7), 431-442 (2002-07-12)
Partial monosomy 10p is a rare chromosomal aberration. Patients often show symptoms of the DiGeorge/velocardiofacial syndrome spectrum. The phenotype is the result of haploinsufficiency of at least two regions on 10p, the HDR1 region associated with hypoparathyroidism, sensorineural deafness, and
Cindy Meyer et al.
Molecular cell, 69(4), 622-635 (2018-02-13)
TIA1 and TIAL1 encode a family of U-rich element mRNA-binding proteins ubiquitously expressed and conserved in metazoans. Using PAR-CLIP, we determined that both proteins bind target sites with identical specificity in 3' UTRs and introns proximal to 5' as well as
Gopal Singh et al.
Nucleic acids research, 32(3), 1232-1241 (2004-02-20)
Members of the CUG-BP and ETR-3 like factor (CELF) protein family bind within conserved intronic elements (called MSEs) flanking the cardiac troponin T (cTNT) alternative exon 5 and promote exon inclusion in vivo and in vitro. Here we use a

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