Fosfo-IRS1 (Tyr632) Polyklonale Antilichaam, Cy7 Vervoeging

Insulin receptor substrates (IRS) are responsible for several insulin related activities, such as glucose homeostasis, cell growth, cell transformation, apoptosis and insulin signal transduction. Serine/threonine phosphorylation of IRS1 has been demonstrated to be a negative regulator of insulin signaling and is responsible for its degradation, although IRS1 degradation pathways are not well understood. IRS1 has also been shown to be constitutively activated in cancers such as breast cancer, Wilm's tumors, and adrenal cortical carcinomas, thus making IRS1 phosphorylation and subsequent degradation an attractive therapeutic target. To date there have been four subtypes identified: IRS1, 2, 3 and 4, with IRS1 being widely expressed.

IRS1 (phospho Tyr632) ; IRS1 (phospho Y632) ; p-IRS1 (phospho Y632) ; HIRS 1; HIRS1; Insulin Receptor Substrate 1; IRS 1; IRS-1; IRS1; IRS1_HUMAN; OTTHUMP00000164234.

3667

P35568

Tyr632

Cell membrane

Human, Mouse, Rat, Bovine, Dog, Pig, Sheep, Rabbit

Phospho-IRS1 (Tyr632)

Cy7

KLH conjugated Synthesised phosphopeptide derived from human IRS1 around the phosphorylation site of Tyr632

IF, Flow-Cyt

Purified by Protein A.

743nm/767nm

1µg/µl

IF (), Flow-Cyt (1ug/Test)

Aqueous buffered solution containing 0.01M TBS (pH 7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Phosphorylation

Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

3667