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Thermo Fisher Scientific BAIAP2 Polyclonal Antibody
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Thermo Fisher Scientific BAIAP2 Polyclonal Antibody

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BAIAP2 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody입니다. WB, IHC, ICC, ELISA 등 다양한 응용에 적합하며, Human, Mouse, Rat 시료에 반응합니다. 고순도 Protein A 정제 및 안정한 액상 형태로 연구용에 최적화되어 있습니다.

카탈로그번호
BS-0242R
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 03:24
Thermo Fisher Scientific BS-0242R BAIAP2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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531,800원VAT 포함 584,980원

Thermo Fisher Scientific · Thermo Fisher Scientific BAIAP2 Polyclonal Antibody

Thermo Fisher Scientific BAIAP2 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC-P) 1:200–1:400
Immunohistochemistry (Frozen) (IHC-F) 1:100–1:500
Immunocytochemistry (ICC/IF) 1:50–1:200
ELISA 1:500–1:1,000

Product Specifications

Property Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen KLH conjugated synthetic peptide derived from human IRS P53, amino acids 151–250
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

The protein encoded by this gene has been identified as a brain-specific angiogenesis inhibitor (BAI1)-binding protein. This adaptor protein links membrane-bound G-proteins to cytoplasmic effector proteins. It functions as an insulin receptor tyrosine kinase substrate and suggests a role for insulin in the central nervous system. It also associates with a downstream effector of Rho small G proteins, which is involved in the formation of stress fibers and cytokinesis. The protein participates in lamellipodia and filopodia formation in motile cells and may affect neuronal growth-cone guidance. Additionally, it interacts with the dentatorubral-pallidoluysian atrophy gene, associated with an autosomal dominant neurodegenerative disease. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

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

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