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Key Documents

MABS1276

Sigma-Aldrich

Anti-TRAP-1 Antibody, clone TR-1

clone TR-1, from mouse

Sinónimos:

Heat shock protein 75 kDa, mitochondrial, TRAP-1, HSP 75, TNFR-associated protein 1, Tumor necrosis factor type 1 receptor-associated protein, TRAP-1

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About This Item

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

biological source

mouse

Quality Level

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

TR-1, monoclonal

species reactivity

human

technique(s)

immunohistochemistry: suitable (paraffin)
immunoprecipitation (IP): suitable
western blot: suitable

isotype

IgG2aκ

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... TRAP1(10131)

General description

Heat shock protein 75 kDa, mitochondrial (UniProt Q12931; also known as HSP 75, TNFR-associated protein 1, TRAP-1, Tumor necrosis factor type 1 receptor-associated protein) is encoded by the TRAP1 (also known as HSP75) gene (Gene ID 10131) in human. The mammalian HSP70 family consists of the mitochondrial HSP75 (TRAP-1), the endoplasmic HSP78, the cytoplasmic HSC70 (a.k.a. HSC73 and HSP73) and its inducible counterpart HSP72 (a.k.a. HSP70). TRAP-1 regulates a metabolic switch between oxidative phosphorylation and aerobic glycolysis. TRAP1-deficiency results in enhanced mitochondrial respiration and fatty acid oxidation, as well as increased cellular accumulation of tricarboxylic acid cycle intermediates, ATP, and reactive oxygen species species. TRAP-1-deficient cells display suppressed glucose metabolism and strikingly enhanced invasiveness, implicating a tumor suppressor role of TRAP-1.

Immunogen

Recombinant protein corresponding to human TRAP-1.

Application

Anti-TRAP-1 Antibody, clone TR-1 is an antibody against TRAP-1 for use in Western Blotting, Immunohistochemistry (Paraffin), Immunoprecipitation.
Immunohistochemistry Analysis: A 1:50 dilution from a representative lot detected TRAP-1 in normal human bladder and human bladder cancer tissue.
Western Blotting Analysis: A representative lot detected TRAP-1 primarily in the inner mitochondrial membrane (IMM) and mitochondrial matrix (Mx), but not the outer mitochondrial membrane (OMM) or the intermembrane space (IMS) of fractionated mitochondria preparations from HeLa cells (Yoshida, S., et al. (2013). Proc. Natl. Acad. Sci. U. S. A. 110(17):E1604-E1612).
Research Category
Signaling

Quality

Evaluated by Western Blotting in HeLa cell lysate.

Western Blotting Analysis: 0.5 µg/mL of this antibody detected TRAP-1 in 10 µg of HeLa cell lysate.

Target description

~75 kDa observed

Physical form

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG2aκ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Storage and Stability

Stable for 1 year at 2-8°C from date of receipt.

Other Notes

Concentration: Please refer to lot specific datasheet.

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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Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

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Kiran Kurmi et al.
Cell metabolism, 28(6), 833-847 (2018-09-04)
How mitochondrial metabolism is altered by oncogenic tyrosine kinases to promote tumor growth is incompletely understood. Here, we show that oncogenic HER2 tyrosine kinase signaling induces phosphorylation of mitochondrial creatine kinase 1 (MtCK1) on tyrosine 153 (Y153) in an ABL-dependent manner

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