CacheBy
Thermo Fisher Scientific CaV2.1 Polyclonal Antibody
원본

Thermo Fisher Scientific CaV2.1 Polyclonal Antibody

상품 한눈에 보기

Rabbit polyclonal antibody targeting human CaV2.1 (CACNA1A) voltage-dependent calcium channel. Detects endogenous total protein. Suitable for IHC and IHC(P). Provided as liquid, unconjugated form, purified by antigen affinity chromatography.

판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 05. 오후 03:17
Thermo Fisher Scientific PA550634 CaV2.1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
630,500원VAT 포함 693,550원

Thermo Fisher Scientific · Thermo Fisher Scientific CaV2.1 Polyclonal Antibody

Applications

Immunohistochemistry (IHC)

Immunohistochemistry (Paraffin) (IHC (P))


Product Specifications

항목 내용
Species Reactivity Human
Published Species Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to internal residues of human calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
Conjugate Unconjugated
Form Liquid
Concentration 1.5 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.4, with 40% glycerol
Contains 0.05% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2636087

Product Specific Information

This antibody detects endogenous levels of total CACNA1A protein.


Target Information

Voltage-dependent calcium channels mediate calcium ion entry into excitable cells and participate in various calcium-dependent processes such as muscle contraction, hormone or neurotransmitter release, and gene expression.
These channels are multisubunit complexes composed of alpha-1, beta, alpha-2/delta, and gamma subunits. The alpha-1 subunit forms the pore and determines channel activity, while auxiliary subunits modulate it.
The alpha-1A subunit, encoded by the CACNA1A gene, is primarily expressed in neuronal tissue. Mutations in this gene are associated with familial hemiplegic migraine and episodic ataxia type 2.
Polymorphic variations due to n-repeats exist in this gene, leading to multiple transcript variants. Expansion of n-repeats in the coding region (from 4–16 to 21–28) causes spinocerebellar ataxia type 6.


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

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.