Anti-phospho-AKT1/2/3 (Thr308)(A16-65M)

Anti-phospho-AKT1/2/3 (Thr308)(A16-65M)

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Description :Mouse Monoclonal Antibody

Species :

Tag :

Expression System:

Sequence :

Specificity :Recognizes the AKT protein phosphorylated at Threonine 308.

Cited Applications :ELISA, IHC, WB
Ideal working dilutions for each application should be empirically determined by the investigator.

Cross Reactivity :Human, Mouse, Rat and Monkey

Host Isotype / Clone# :Mouse, IgG

Immunogen :The antibody was produced against synthesized peptide corresponding to residues surrounding Thr 308 of Human AKT1 protein.

Purification :Protein A Chromatography

Stability :1yr at –20oC from date of shipment

Sample Data :Immunohistochemical analysis of formalin fixed, paraffin embedded human brain cerebellum tissue (40x) using Anti-Phospho-ATK1/2/3 (Thr308)

Sample Data :Western Blot of Anti-Phospho-AKT1/2/3 (Thr308) (1:4,000). Lane 1: non-phosphorylated AKT in untreated cells . Lane 2: phosphorylated AKT on PDGF stimulated NIH/3T3 cell lysates . Load: 15 µg per lane.

Scientific Background :AKT1/PKBα is a serine/threonine kinase that belongs to the AKT family. AKT1 is activated in cells in response to diverse stimuli such as hormones, growth factors and extracellular matrix components and is involved in glucose metabolism, transcription, survival, cell proliferation, angiogenesis, and cell motility (1). AKT1 is frequently overexpressed and active in many types of human cancers including cancers of colon, breast, brain, pancreas and prostate as well as lymphomas and leukemias (2).

References :
1. Coffer, PJ. et al: Protein kinase B (c-Akt): a multifunctional mediator of phosphatidylinositol 3-kinase activation. Biochem J. 1998 Oct 1; 369 ( Pt 1):1-13. 

2. Anderson, KE. et al: Translocation of PDK-1 to the plasma membrane is important in allowing PDK-1 to activate protein kinase B. Curr Biol. 1998 Jun 4;8(12): 684-91.

Product Sheets (By Lot #) :

B3216-13.pdf

Research Areas :AKT/PKB Pathway, Angiogenesis, Apoptosis/Autophagy, Cancer, Cardiovascular Disease, Inflammation, Invasion/Metastasis, Metabolic Disorder, Neurobiology, NfkB Pathway, WNT Signaling