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Merck
CN

GW22763

Anti-GAPDH antibody produced in chicken

affinity isolated antibody, buffered aqueous solution

别名:

Gapdh Antibody Sigma, Gapdh Antibody Sigma - Anti-GAPDH antibody produced in chicken

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关于此项目

UNSPSC Code:
12352203
MDL number:
Conjugate:
unconjugated
Clone:
polyclonal
Application:
WB
Citations:
10
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biological source

chicken

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

species reactivity

rat, mouse, human

manufacturer/tradename

Genway 15-288-22763

technique(s)

western blot: suitable

NCBI accession no.

UniProt accession no.

shipped in

wet ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... GAPDH(2597)

Immunogen

Immunogen Sequence: GI # 7669492, sequence 51-290
Recombinant glyceraldehyde-3-phosphate dehydrogenase

Application

Anti-GAPDH antibody produced in chicken is suitable for western blotting analysis at a dilution of 1:500, for tissue or cell staining at a dilution of 1:200.
Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Western Blotting (1 paper)

Biochem/physiol Actions

Glyceraldehyde 3-phosphate dehydrogenase (G3PDH) is an enzyme that catalyzes the sixth step of glycolysis and serves to break down glucose for energy and carbon molecules. It is an obligatory enzyme in glycolysis and performs a critical role in cellular regulation. GAPDH also plays a critical role in apoptosis and age-related neurodegenerative diseases, such as Alzheimer′s, Huntington′s and Parkinson′s diseases. Overexpression of this gene in resected tumor samples is an adverse prognostic factor in non-small cell lung cancers (NSCLC). It is used as a stable housekeeping marker for constant gene expression and its transcriptional levels may be highly up-regulated in some cancers.

Physical form

Solution in phosphate buffered saline containing 0.02% sodium azide.

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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wgk

WGK 1

存储类别

12 - Non Combustible Liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

法规信息

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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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Feng Zhao et al.
Oncology letters, 9(1), 159-164 (2014-12-02)
Hypermethylated in cancer 1 (HIC-1) is a tumor suppressor gene, which is epigenetically silenced in breast cancer. It is known that the loss of HIC-1, caused by promoter hypermethylation, is associated with tumor aggression and poor survival in breast carcinoma.
Roberto Puzone et al.
Molecular cancer, 12(1), 97-97 (2013-08-31)
Glycolysis in presence of oxygen with high glucose consumption is known to be the metabolism of choice in many tumors. In lung cancer this phenomenon is routinely exploited in diagnostic PET imaging of fluorodeoxyglucose uptake, but not much is known
Aleksandra Rodacka
Postepy higieny i medycyny doswiadczalnej (Online), 67, 775-789 (2013-09-11)
For a long time glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was considered a classical glycolytic protein of little interest. It was also used as a model protein for analysis of protein structure and enzyme mechanisms. However, recent evidence demonstrates that GAPDH from mammalian
Tingting Li et al.
The Journal of biological chemistry, 289(6), 3775-3785 (2013-12-24)
The altered metabolism in most tumor cells consists of elevated glucose uptake and increased glycolysis even in the presence of high oxygen tension. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is an obligatory enzyme in glycolysis. Here, we report that acetylation at lysine 254
Andres E Perez Bay et al.
Nature communications, 7, 11550-11550 (2016-05-18)
The basolateral recycling and transcytotic pathways of epithelial cells were previously defined using markers such as transferrin (TfR) and polymeric IgA (pIgR) receptors. In contrast, our knowledge of the apical recycling pathway remains fragmentary. Here we utilize quantitative live-imaging and

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