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Merck
CN

I1658

Anti-phospho-Insulin Receptor Substrate-1 (pTyr1179) antibody produced in rabbit

affinity isolated antibody, buffered aqueous solution

别名:

Anti-phospho-IRS-1 (pTyr1179)

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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

buffered aqueous solution

species reactivity

human, rat, mouse

technique(s)

western blot: 0.1-1.0 μg/mL using stimulated CHO cell line

UniProt accession no.

shipped in

dry ice

storage temp.

−70°C

Gene Information

human ... IRS1(3667)
mouse ... Irs1(16367)
rat ... Irs1(25467)

General description

Insulin receptor substrate-1 (IRS-1) is among the four IRS proteins (IRS-1-IRS-4) that mediate signalling by insulin receptor (IR) and insulin-like growth factor (IGF) receptor. IRS-1 has a pleckstrin homology domain and a phosphotyrosine-binding domain. Phosphorylation of the Tyr1179 residue in the SH-1 negatively regulates insulin. IRS-1 has the abililty to translocate to the nucleus, the mechanism of which is not very clear. Estrogen receptors (ER) α and β have a strong affinity to IRS-1, an important interaction in breast cancers and medulloblastomas. The expression of IRS-1 in prostate cancer is associated with lower tumor cell invasiveness. Along with ER α, IRS-1 also modulates transcriptional activity involved in the development of breast and prostate cancer. The signalling pathway involving IGF-IR-IRS-1 in cells expressing JCV T-antigen has been reported to affect the proliferation, survival and DNA repair in the cells
Anti-phospho-IRS-1 (pTyr1179) specifically recognizes human IRS-1 (pTyr1179). It may react with mouse (100% homology) and rat (93% homology) IRS-1.

Immunogen

synthetic phosphopeptide derived from the region of mouse insulin receptor substrate-1 that is phosphorylated on tyrosine 1173 (corresponding to tyrosine 1179 of the human sequence).

Application

Anti-phospho-IRS-1 (pTyr1179) antibody may be used for detection by immunoblotting, in stimulated CHO cell line, at a working concentration of 0.1 to 1.0 μg/ml.

Physical form

Solution in phosphate buffered saline, pH 7.3, containing 1 mg/mL BSA (IgG and protease free) and 0.05% 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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存储类别

12 - Non Combustible Liquids

wgk

WGK 1

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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分析证书(COA)

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W Ogawa et al.
Molecular and cellular biochemistry, 182(1-2), 13-22 (1998-06-03)
Insulin elicits its divergent metabolic and mitogenic effects by binding to its specific receptor, which belongs to the family of receptor tyrosine kinases. The activated insulin receptor phosphorylates the intracellular substrate IRS-1, which then binds various signalling molecules that contain
Catia Morelli et al.
Oncogene, 23(45), 7517-7526 (2004-08-20)
Insulin receptor substrate 1 (IRS-1) is a major signaling molecule activated by the insulin and insulin-like growth factor I receptors. Recent data obtained in different cell models suggested that in addition to its conventional role as a cytoplasmic signal transducer
Krzysztof Reiss et al.
Journal of cellular physiology, 227(8), 2992-3000 (2012-03-29)
The family of insulin receptor substrates (IRS) consists of four proteins (IRS-1-IRS-4), which were initially characterized as typical cytosolic adaptor proteins involved in insulin receptor (IR) and insulin-like growth factor I receptor (IGF-IR) signaling. The first cloned and characterized member
K Reiss et al.
Oncogene, 20(4), 490-500 (2001-04-21)
LNCaP cells are human prostatic cancer cells that have a frame-shift mutation of the tumor suppressor gene PTEN and do not express the insulin receptor substrate-1 (IRS-1), a major substrate of the type 1 insulin-like growth factor receptor (IGF-IR). Ectopic
Catia Morelli et al.
Oncogene, 22(26), 4007-4016 (2003-06-25)
In breast cancer cells, 17-beta-estradiol (E2) upregulates the expression of insulin receptor substrate 1 (IRS-1), a molecule transmitting insulin-like growth factor-I (IGF-I) signals through the PI-3K/Akt survival pathways. The stimulation of IRS-1 by E2 has been documented on the transcriptional

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