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Merck
CN

SAB2103104

Anti-GAPDH antibody produced in rabbit

affinity isolated antibody, lyophilized powder

别名:

Anti-G3PD, Anti-GAPD, Anti-MGC88685

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关于此项目

UNSPSC Code:
12352203
MDL number:
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biological source

rabbit

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

lyophilized powder

mol wt

36 kDa

species reactivity

mouse, rat, rabbit, human, horse, pig

technique(s)

western blot: suitable

immunogen sequence

KAGAHLQGGAKRVIISAPSADAPMFVMGVNHEKYDNSLKIISNASCTTNC

NCBI accession no.

UniProt accession no.

storage temp.

−20°C

Gene Information

human ... GAPDH(2597)

Immunogen

Peptide region of the protein sequence according to NP_002037.

Application

Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Western Blotting (1 paper)

Physical form

Antibody is lyophilized from PBS buffer with 2% sucrose.

Disclaimer

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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存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

常规特殊物品

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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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Yang Fu et al.
Molecular carcinogenesis, 58(11), 2104-2117 (2019-08-31)
Small nucleolar RNA host gene 1 (SNHG1) is critical in the progression of cancers. However, the mechanism by which SNHG1 regulates the progression of colorectal cancer (CRC) remains unclear. Expressions of SNHG1 and miR-137 in CRC tissues and cell lines
Theodore G Drivas et al.
The Journal of clinical investigation, 123(10), 4525-4539 (2013-09-21)
Mutations in the gene centrosomal protein 290 kDa (CEP290) cause an array of debilitating and phenotypically distinct human diseases, ranging from the devastating blinding disease Leber congenital amaurosis (LCA) to Senior-Løken syndrome, Joubert syndrome, and the lethal Meckel-Gruber syndrome. Despite
Ke Xu et al.
Journal of neurochemistry, 149(6), 799-810 (2018-12-07)
The proportion of major depressive disorder (MDD) patients around the world has increased remarkably. Although many studies of MDD have been conducted based on classic hypotheses, like alteration of the hypothalamic-pituitary-adrenal axis or monoamine neurotransmitters, the mechanisms underlying MDD remain