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Thermo Fisher Scientific Phospho-AKT1 (Thr34) Polyclonal Antibody
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Thermo Fisher Scientific Phospho-AKT1 (Thr34) Polyclonal Antibody

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AKT1 Thr34 인산화 상태를 검출하는 Rabbit Polyclonal Antibody. Western blot, IHC, ICC, Flow, ELISA 등 다양한 응용에 적합. Human, Mouse, Rat 반응성. 고순도 Protein A 정제, 안정적 액상 형태로 -20°C 보관.

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마지막 업데이트 2025. 08. 03. 오후 09:27
Thermo Fisher Scientific BS-5194R Phospho-AKT1 (Thr34) Polyclonal Antibody 100 ul pk판매 단위 pk ·
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590,500원VAT 포함 649,550원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-AKT1 (Thr34) Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:300
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent
Immunohistochemistry (Frozen) (IHC (F)) 1:100–1:500
Immunocytochemistry (ICC/IF) 1:50–1:200
Flow Cytometry (Flow) 1:20–1:100
ELISA 1:500–1:1,000

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen KLH-conjugated synthetic phosphopeptide derived from human AKT1 around the phosphorylation site of Thr34
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer 0.01M TBS, pH 7.4, with 50% glycerol, 1% BSA
Contains 0.02% ProClin 300
Storage Conditions -20°C
Shipping Conditions Ambient (domestic); Wet ice (international)

Target Information

AKT1 (PKB alpha) is a serine/threonine kinase that regulates cell survival. The activated enzyme inhibits apoptosis and stimulates cell cycle progression by phosphorylating numerous targets in various cell types, including cancer cells. This protein kinase is activated by insulin, PI3K, IGF1 and various other growth and survival factors. Akt promotes cell survival by inhibiting apoptosis through phosphorylation and inactivation of several targets, including forkhead transcription factors and caspase-9. The AKT pathway is a major target for cancer drug discovery.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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