CacheBy
Thermo Fisher Scientific Spectrin beta III (SPTBN2) Monoclonal Antibody (SPTBN2/1778)
원본

Thermo Fisher Scientific Spectrin beta III (SPTBN2) Monoclonal Antibody (SPTBN2/1778)

상품 한눈에 보기

인간 SPTBN2 단백질을 인식하는 mouse monoclonal 항체로, WB, IHC, ICC 등 다양한 응용에 사용 가능. Protein A/G 정제, 200 µg/mL 농도의 액상 형태. 세포막-세포골격 관련 연구 및 신경퇴행 질환 연구에 적합.

판매단위
pk
카탈로그 보기

카탈로그

2개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
ADRepligen 웨비나PATsmart를 활용한 바이오공정 분석 전략 · 10/7 오전 10시자세히보기
Thermo Fisher Scientific 6712-MSM5-P1 Spectrin beta III (SPTBN2) Monoclonal Antibody (SPTBN2/1778) 100 ug pk판매 단위 pk
재고 확인 필요
900,300원VAT 포함 990,330원
Thermo Fisher Scientific 6712-MSM5-P0 Spectrin beta III (SPTBN2) Monoclonal Antibody (SPTBN2/1778) 20 ug pk판매 단위 pk
재고 확인 필요
449,700원VAT 포함 494,670원

Thermo Fisher Scientific · Thermo Fisher Scientific Spectrin beta III (SPTBN2) Monoclonal Antibody (SPTBN2/1778)

Applications and Tested Dilutions

Application Tested Dilution Notes
Western Blot (WB) 1–2 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1–2 µg/mL
Immunocytochemistry (ICC/IF) 2–4 µg/mL
Peptide Array (Array) Assay-dependent

Product Specifications

Specification Detail
Species Reactivity Human
Host / Isotype Mouse / IgG1, kappa
Class Monoclonal
Type Antibody
Clone SPTBN2/1778
Immunogen Recombinant fragment (around aa356–475) of human SPTBN2 protein
Conjugate Unconjugated
Form Liquid
Concentration 200 µg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4, with 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions 4°C, do not freeze
Shipping Conditions Ambient (domestic); Wet ice (international)

Target Information

Spectrins are principal components of the cell membrane-cytoskeleton and are composed of two alpha and two beta spectrin subunits.
The protein encoded by the SPTBN2 gene, known as spectrin beta non-erythrocytic 2 or beta-III spectrin, is related to but distinct from beta-II spectrin (SPTBN1).
SPTBN2 regulates the glutamate signaling pathway by stabilizing the glutamate transporter EAAT4 at the plasma membrane surface.
Mutations in this gene cause spinocerebellar ataxia type 5 (SCA5), characterized by neurodegeneration, locomotor incoordination, dysarthria, and uncoordinated eye movements.


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

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0개

아직 등록된 문의가 없어요.