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Thermo Fisher Scientific Spectrin beta III (SPTBN2) Recombinant Rabbit Monoclonal Antibody (SPTBN2/2979R)
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Thermo Fisher Scientific Spectrin beta III (SPTBN2) Recombinant Rabbit Monoclonal Antibody (SPTBN2/2979R)

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Spectrin beta III(SPTBN2) 단백질을 타겟으로 하는 Thermo Fisher의 재조합 토끼 단일클론 항체. Western blot 및 면역조직화학(IHC) 분석에 적합하며, 인간, 생쥐, 랫트 시료에 반응. Protein A/G 정제, 4°C 보관.

카탈로그번호
6712-RBM8-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-RBM8-P1 Spectrin beta III (SPTBN2) Recombinant Rabbit Monoclonal Antibody (SPTBN2/2979R) 100 ug pk판매 단위 pk ·
재고 확인 필요
1,063,800원VAT 포함 1,170,180원
Thermo Fisher Scientific 6712-RBM8-P0 Spectrin beta III (SPTBN2) Recombinant Rabbit Monoclonal Antibody (SPTBN2/2979R) 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 (SPTBN2/2979R)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1–2 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone SPTBN2/2979R
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, composed of two alpha and two beta spectrin subunits. The SPTBN2 gene encodes spectrin beta non-erythrocytic 2 (beta-III spectrin), which 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 SPTBN2 cause 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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