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Phospho-AKT1 (S124) Monoclonal Antibody

Product Specifications

Background

The serine-threonine protein kinase encoded by the AKT1 gene is catalytically inactive in serum-starved primary and immortalized fibroblasts. AKT1 and the related AKT2 are activated by platelet-derived growth factor. The activation is rapid and specific, and it is abrogated by mutations in the pleckstrin homology domain of AKT1. It was shown that the activation occurs through phosphatidylinositol 3-kinase. In the developing nervous system AKT is a critical mediator of growth factor-induced neuronal survival. Survival factors can suppress apoptosis in a transcription-independent manner by activating the serine/threonine kinase AKT1, which then phosphorylates and inactivates components of the apoptotic machinery. Mutations in this gene have been associated with the Proteus syndrome. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2011]

Synonyms

AKT 1 antibody, AKT antibody, AKT1 antibody, AKT1_HUMAN antibody, MGC99656 antibody, PKB antibody, PKB-ALPHA antibody, PRKBA antibody, Protein Kinase B Alpha antibody, Protein kinase B antibody, Proto-oncogene c-Akt antibody, RAC Alpha antibody, RAC antibody, RAC-alpha serine/threonine-protein kinase antibody, RAC-PK-alpha antibody

Gene ID

207

Swiss Prot

P31749

Modification Site

Ser124

Cellular Locus

Cytoplasm, Nucleus, Cell membrane

Host

Rabbit

Cross Reactivity

Human, Mouse, Rat

Target

Phospho-AKT1 (S124)

Clonality

Monoclonal

Isotype

IgG

Clone

2F2

Conjugation

Unconjugated

Source

Synthetic phospho-Peptide corresponding to residues surrounding Ser124 of human AKT1.

Applications

WB, IHC-P, IF (ICC), IP, IHC

Purification

Purified by Protein A.

Concentration

1µg/µl

Dilution

WB (1:300-5000), IHC-P (1:200-400), IF (ICC) (1:50-200), IP (1-2ug), IHC ()

Buffer

0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Modification

Phosphorylation

Storage Conditions

Store at -20°C for 12 months.

Gene ID URL

207

Frequently Asked Questions

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