Insulin Receptor Substrate 1 Phospho-Tyr896 (IRS1 pY896) Antibody

Este producto es parte de IRS -Insulin receptor substrate
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221€ (50 µg)

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935106861
info@markelab.com
name
Insulin Receptor Substrate 1 Phospho-Tyr896 (IRS1 pY896) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx327747
tested applications
ELISA, WB

Description

IRS1 (pY896) Antibody is a Rabbit Polyclonal against IRS1 (pY896).

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Insulin Receptor Substrate 1 Phospho-Tyr896 (IRS1 pY896)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Assay Data
Modification: Phosphorylation // Target Modification: Tyr896
Recommended Dilution
ELISA: 1/40000, WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
50 µg
Size 2
100 µg
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P35568
Gene ID
3667
Alias
IRS1, HIRS-1, insulin receptor substrate 1
Background
Antibody anti-IRS1
Status
RUO

Descripción

IRS1 is a key adaptor protein that mediates insulin and insulin-like growth factor (IGF) signaling by interacting with the insulin receptor (IR) and IGF-1 receptor. Upon receptor activation, IRS1 is phosphorylated on tyrosine residues, recruiting downstream effectors such as PI3K and Grb2 to activate pathways like PI3K/Akt and Ras/MAPK. IRS1 regulates glucose uptake, metabolism, cell growth, and survival, playing a central role in insulin signaling. It is highly expressed in insulin-sensitive tissues like muscle, liver, and adipose. Dysregulation of IRS1 is associated with insulin resistance, obesity, type 2 diabetes, and cancer, where aberrant signaling promotes proliferation and survival. Knockout studies show growth retardation, metabolic abnormalities, and impaired glucose homeostasis, underscoring its importance in metabolism and cellular signaling.

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