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ELK Biotechnology Akt1 (phospho Thr72) rabbit pAb
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ELK Biotechnology Akt1 (phospho Thr72) rabbit pAb

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Akt1 (phospho Thr72) rabbit pAb는 인간, 마우스, 랫트에서 반응하는 다클론 항체로 WB, IHC, IF, ELISA에 사용 가능합니다. Thr72 인산화 부위 기반으로 제작되었으며, 세포질과 핵에서 발현된 Akt1 검출에 적합합니다. -20°C 보관 시 1년 안정합니다.

카탈로그번호
ES5160-xxxxx (2개 옵션)
판매단위
pk
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2개 옵션
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ELK Biotechnology ES5160-100UL Akt1 (phospho Thr72) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES5160-50UL Akt1 (phospho Thr72) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology Akt1 (phospho Thr72) rabbit pAb

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Akt1 (phospho Thr72) rabbit pAb

제품 정보

항목 내용
Alternative Names AKT1; PKB; RAC; RAC-alpha serine/threonine-protein kinase; Protein kinase B; PKB alpha; Proto-oncogene c-Akt; RAC-PK-alpha
Applications WB; IHC; IF; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
Immunohistochemistry: 1/100 - 1/300
ELISA: 1/5000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human Akt around the phosphorylation site of Thr72 (AA range: 38–87)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 56 kDa
Gene ID (Human) 207
Human Swiss-Prot No. P31749
Species Reactivity Human; Mouse; Rat
Cellular Localization Cytoplasm, Nucleus, Cell membrane. Translocates to the nucleus after activation by ILK1. Localization to the membrane is enhanced by phosphorylation on Tyr-176 by TNK2, leading to subsequent phosphorylations on Thr-308 and Ser-473 for activation. Colocalizes with WDFY2 in intracellular vesicles (PubMed:16792529).

Background

The serine-threonine protein kinase encoded by the AKT1 gene is catalytically inactive in serum-starved fibroblasts. AKT1 and AKT2 are activated by platelet-derived growth factor through a phosphatidylinositol 3-kinase-dependent mechanism.
In the developing nervous system, AKT1 acts as a critical mediator of growth factor-induced neuronal survival. It suppresses apoptosis by phosphorylating and inactivating apoptotic components in a transcription-independent manner.
Mutations in this gene are associated with Proteus syndrome, and multiple alternatively spliced transcript variants have been identified (RefSeq, Jul 2011).

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