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Thermo Fisher Scientific AKT1 Monoclonal Antibody (OTI4E10), TrueMAB
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Thermo Fisher Scientific AKT1 Monoclonal Antibody (OTI4E10), TrueMAB

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AKT1 단백질을 인식하는 Mouse Monoclonal Antibody (Clone OTI4E10). Western blot, IHC, ICC/IF, Flow Cytometry에 사용 가능. 인간, 마우스, 랫, 개 시료 반응. 액상형, 1 mg/mL, PBS/BSA/glycerol buffer. 연구용 전용.

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마지막 업데이트 2025. 07. 30. 오후 09:24
Thermo Fisher Scientific TA504234 AKT1 Monoclonal Antibody (OTI4E10), TrueMAB 100 ul pk판매 단위 pk ·
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600,200원VAT 포함 660,220원

Thermo Fisher Scientific · Thermo Fisher Scientific AKT1 Monoclonal Antibody (OTI4E10), TrueMAB

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC-P) 1:150
Immunocytochemistry (ICC/IF) 1:100
Flow Cytometry (Flow) 1:100
Miscellaneous PubMed (Misc) -

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Product Specifications

항목 내용
Species Reactivity Dog, Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI4E10
Immunogen Full length human recombinant protein of human AKT1 produced in HEK293T cell
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS with 1% BSA, 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
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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