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Thermo Fisher Scientific Spectrin beta III (SPTBN2) Recombinant Rabbit Monoclonal Antibody (SPTBN2/2887R)
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Thermo Fisher Scientific Spectrin beta III (SPTBN2) Recombinant Rabbit Monoclonal Antibody (SPTBN2/2887R)

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Spectrin beta III(SPTBN2)에 특이적인 재조합 토끼 단일클론 항체로, WB, IHC, ICC/IF, Flow Cytometry에 사용 가능. HEK293 발현 시스템 기반, Protein A/G 정제, 200 µg/mL 농도. 인간 시료 반응성, 연구용 전용.

카탈로그번호
6712-RBM6-Px (2개 옵션)
판매단위
pk
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2개 옵션
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마지막 업데이트 2025. 08. 02. 오후 01:09
Thermo Fisher Scientific 6712-RBM6-P1 Spectrin beta III (SPTBN2) Recombinant Rabbit Monoclonal Antibody (SPTBN2/2887R) 100 ug pk판매 단위 pk ·
재고 확인 필요
1,063,800원VAT 포함 1,170,180원
Thermo Fisher Scientific 6712-RBM6-P0 Spectrin beta III (SPTBN2) Recombinant Rabbit Monoclonal Antibody (SPTBN2/2887R) 20 ug pk판매 단위 pk ·
재고 확인 필요
452,600원VAT 포함 497,860원

Thermo Fisher Scientific · Thermo Fisher Scientific Spectrin beta III (SPTBN2) Recombinant Rabbit Monoclonal Antibody (SPTBN2/2887R)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1–2 µg/mL
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1–2 µg/mL
Immunocytochemistry (ICC/IF) 1–2 µg/mL
Flow Cytometry (Flow) 1–2 µg/10^6 cells

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone SPTBN2/2887R
Immunogen Recombinant human SPTBN2 fragment (aa356–475)
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 consist of two alpha and two beta spectrin subunits. The protein encoded by the SPTBN2 gene, also 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 are associated with spinocerebellar ataxia type 5 (SCA5), characterized by neurodegeneration, progressive locomotor incoordination, dysarthria, and uncoordinated eye movements.


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

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