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MAB1137Z

Sigma-Aldrich

Anti-Insulin Receptor Antibody, α subunit, azide free, clone 47-9

clone 47-9, Chemicon®, from mouse

Sinónimos:

CD220, MAB1137

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About This Item

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

origen biológico

mouse

forma del anticuerpo

purified immunoglobulin

tipo de anticuerpo

primary antibodies

clon

47-9, monoclonal

reactividad de especies

human, pig, sheep, bovine

no debe reaccionar con

rat, mouse

fabricante / nombre comercial

Chemicon®

isotipo

IgG1

idoneidad

not suitable for Western blot
not suitable for immunoprecipitation

Nº de acceso NCBI

Nº de acceso UniProt

Condiciones de envío

wet ice

modificación del objetivo postraduccional

unmodified

Información sobre el gen

human ... INSR(3643)

Especificidad

Recognizes a protein of 135kDa, identified as the alpha-subunit of insulin receptor (IR). Its epitope localizes in exon 7/8 and shows no cross-reaction with IGF-receptors {Soos, 1986}. Antibody superbly inhibits (>90%) insulin binding and BLOCKS insulin action. IR is a heterotetrameric membrane glycoprotein consisting of disulfide-linked subunits in a beta-a-a-beta configuration. The beta-subunit (95kDa) possesses a single transmembrane domain, whereas the alpha-subunit is completely extracellular. The intracellular portion of the beta-subunit is a tyrosine-specific protein kinase with sequence homology to other such kinases. Activation of kinase is essential in signaling pathway whereby insulin regulates intracellular metabolism.

Inmunógeno

Epitope: alpha subunit, azide free
IM-9 lymphocytes followed by purified insulin receptor.

Aplicación

Anti-Insulin Receptor Antibody, α subunit, azide free, clone 47-9 detects level of Insulin Receptor & has been published & validated.
Completely (>90%) Inhibits Insulin Binding: use antibody at 10nM

Antagonist: Blocks insulin action

Does not work in immunoprecipitation {Soos, 1986}.

Optimal working dilutions must be determined by end user.
Research Category
Signaling
Research Sub Category
Insulin/Energy Signaling

Forma física

Format: Purified
Protein G Purified
Protein G Purified mouse immunoglobulin in 10mM PBS, pH 7.4 contain no preservatives.

Almacenamiento y estabilidad

Maintain for 2 years at -20°C from date of shipment. Aliquot to avoid repeated freezing and thawing. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.

Nota de análisis

Control
3T3 cells expressing transfected human insulin receptor

Otras notas

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Información legal

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

Cláusula de descargo de responsabilidad

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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Código de clase de almacenamiento

12 - Non Combustible Liquids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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The Garcia effect, a solid learning paradigm, was used to investigate the molecular and behavioral effects induced by different lengths of fasting on the cognitive functions in the pond snail Lymnaea stagnalis, a valid model system. Three experimental groups were
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The Journal of clinical endocrinology and metabolism, 108(9), 2324-2329 (2023-03-05)
Severe insulin resistance (IR) in the presence of insulin receptor autoantibodies (InsR-aAb) is known as type B insulin resistance (TBIR). Considerable progress in therapy has been achieved, but diagnosis and monitoring of InsR-aAb remains a challenge. This work aimed to
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Insulin is present in most maintenance media for human embryonic stem cells (hESCs), but little is known about its essential role in the cell survival of individualized cells during passage. In this article, we show that insulin suppresses caspase cleavage

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