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Merck
CN

GR36

Anti-Insulin Receptor (β-Subunit) Mouse mAb (CT-3)

liquid, clone CT-3, Calbiochem®

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UNSPSC Code:
12352203
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biological source

mouse

antibody product type

primary antibodies

clone

CT-3, monoclonal

form

liquid

contains

≤0.1% sodium azide as preservative

species reactivity

mouse, human, rat

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, avoid repeated freeze/thaw cycles

isotype

IgG1

shipped in

wet ice

Quality Level

General description

Purified mouse monoclonal antibody gernerated by immunizing BALB/c mice with the specified immunogen and fusing splenocytes with NS1 mouse myeloma cells. Recognizes the ~95 kDa the β-subunit of insulin receptor.
Recognizes the ~95 kDa the β-subunit of insulin receptor in IM9 cells, placenta, and fetal liver tissue.
This Anti-Insulin Receptor (β-Subunit) Mouse mAb (CT-3) is validated for use in Frozen Sections, Immunoblotting, IP, Paraffin Sections for the detection of Insulin Receptor (β-Subunit).

Immunogen

Human
a recombinant protein consisting of the C-terminal 100 amino acids of the β-subunit of human insulin receptor fused to GST

Application



Frozen Sections (1:50-1:100)

Immunoblotting (1:200-1:400)

Immunoprecipitation (not recommended)

Paraffin Sections (1:50-1:100, pressure cooker pre-treatment required)

Packaging

Please refer to vial label for lot-specific concentration.

Physical form

In 10 mM PBS, 0.2% BSA, pH 7.4.

Preparation Note

Following initial use, aliquot and freeze (-20°C) for long-term storage. Avoid freeze/thaw cycles. Centrifuge the contents of the vial containing the antibody before use to remove any solution that may have accumulated around or under the cap of the vial during shipment or storage.

Analysis Note

Positive Control
IM-9 lymphocyte cells or placenta or liver tissue

Other Notes

Grigorescu, F., et al. 1987. J.Clin. Endocrinol. Metab.64, 549.
Hari, J. and Roth, R.A. 1987. J. Biol. Chem.262, 15341.
Rosen, O.M. 1987. Science237, 1452.
Morgan, D.O., et al. 1986. Proc. Natl. Acad. Sci. USA83, 328.
Morgan, D.O. and Roth, R.A. 1986. Biochemistry25, 1364.
White, M.F. and Kahn, C.R. 1986. The Enzymes17, 247.
Ganguly, S., et al. 1985. In Current Topics in Cellular Regulation, Academic Press 27, 83.
Grunberger, G., et al. 1984. Science223, 932.
No cross-reactivity with IGF receptors. Will stain IM-9 lymphocyte cells as well as placenta and liver tissue. This antibody is also useful for tyrosine kinase assays for antibody mediated capture on microwell plates. Antibody should be titrated for optimal results in individual systems.

Legal Information

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

Disclaimer

Toxicity: Standard Handling (A)

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存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Raju V S Rajala et al.
The Journal of biological chemistry, 277(45), 43319-43326 (2002-09-06)
Recently, we have shown that phosphoinositide 3-kinase (PI3K) in bovine rod outer segment (ROS) is activated in vitro by tyrosine phosphorylation of the C-terminal tail of the insulin receptor (Rajala, R. V. S., and Anderson, R. E. (2001) Invest. Ophthal.
Jennifer H Law et al.
Cancer research, 68(24), 10238-10246 (2008-12-17)
Drugs that target the insulin-like growth factor-I receptor (IGF-IR) and/or insulin receptor (IR) are currently under investigation for a variety of malignancies including breast cancer. Although we have previously reported that IGF-IR expression in primary breast tumors is common, the
Sofie Björner et al.
Oncotarget, 8(6), 9093-9107 (2016-12-29)
Clinical trials examining insulin-like growth factor-I receptor (IGF1R)-targeting strategies have emphasized that better predictive biomarkers are required to improve patient selection.Immunohistochemical tumor-specific protein expression of IGF1R, insulin receptor (InsR), and phosphorylated IGF1R/InsR (pIGF1R/InsR) individually and combined in relation to breast
Sofie Björner et al.
Frontiers in endocrinology, 8, 332-332 (2017-12-14)
The prognostic importance of tumor-specific nuclear insulin receptor (InsR) expression in breast cancer is unclear, while membrane and cytoplasmic localization of InsR is better characterized. The insulin signaling network is influenced by obesity and may interact with the estrogen receptor
Henning Hvid et al.
Journal of applied toxicology : JAT, 31(4), 312-328 (2011-01-25)
Supra-pharmacological doses of the insulin analog X10 (AspB10) increased the incidence of mammary tumors in female Sprague-Dawley rats in chronic toxicity studies, most likely via receptor-mediated mechanisms. However, little is known about the expression of the insulin receptor family in

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