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

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
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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