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SPTN2 rabbit pAb
商品貨號: PLA020768
適 應(yīng) 性: 人,大鼠
WB IHC
¥600元
規(guī)格:
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MSDS
說明書
商品描述
  • 基因名稱: SPTBN2 KIAA0302 SCA5
  • 蛋白名稱: SPTN2
  • Human_gene_id: 6712
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6712
  • Human_swiss_prot_no: O15020
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/O15020/entry
  • Rat_gene_id: 29211
  • Rat_gene_link: https://www.uniprot.org/uniprot/29211
  • Rat_swiss_prot_no: Q9QWN8
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/Q9QWN8
  • 特異性: This antibody detects endogenous levels of SPTN2 at Human/Rat
  • 組成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源: Polyclonal, Rabbit,IgG
  • 稀釋: WB 1:500-2000;IHC-p 1:50-300
  • 純化工藝: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度: 1 mg/ml
  • 儲存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 263kD
  • 功能: disease:Defects in SPTBN2 are the cause of spinocerebellar ataxia type 5 (SCA5) [MIM:600224]. Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA5 is an autosomal dominant cerebellar ataxia (ADCA). It is a slowly progressive disorder with variable age at onset, ranging between 10 and 50 years.,function:Probably plays an important role in neuronal membrane skeleton.,similarity:Belongs to the spectrin family.,similarity:Contains 1 PH domain.,similarity:Contains 17 spectrin repeats.,similarity:Contains 2 CH (calponin-homology) domains.,tissue specificity:Highly expressed in brain, kidney, pancreas, and liver, and at lower levels in lung and placenta.,
  • 相關(guān)產(chǎn)品: RS0001,RS0002,YM3028,YM3029
  • 細(xì)胞定位: Cytoplasm, cytoskeleton. Cytoplasm, cell cortex.
  • 組織表達(dá): Highly expressed in brain, kidney, pancreas, and liver, and at lower levels in lung and placenta.
  • 科研貨號: PLA020768
SPTN2 rabbit pAb
Catalog No PLA020768
Product information
  • 基因名稱: SPTBN2 KIAA0302 SCA5
  • 蛋白名稱: SPTN2
  • Human_gene_id: 6712
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6712
  • Human_swiss_prot_no: O15020
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/O15020/entry
  • Rat_gene_id: 29211
  • Rat_gene_link: https://www.uniprot.org/uniprot/29211
  • Rat_swiss_prot_no: Q9QWN8
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/Q9QWN8
  • 特異性: This antibody detects endogenous levels of SPTN2 at Human/Rat
  • 組成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源: Polyclonal, Rabbit,IgG
  • 稀釋: WB 1:500-2000;IHC-p 1:50-300
  • 純化工藝: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度: 1 mg/ml
  • 儲存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 263kD
  • 功能: disease:Defects in SPTBN2 are the cause of spinocerebellar ataxia type 5 (SCA5) [MIM:600224]. Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA5 is an autosomal dominant cerebellar ataxia (ADCA). It is a slowly progressive disorder with variable age at onset, ranging between 10 and 50 years.,function:Probably plays an important role in neuronal membrane skeleton.,similarity:Belongs to the spectrin family.,similarity:Contains 1 PH domain.,similarity:Contains 17 spectrin repeats.,similarity:Contains 2 CH (calponin-homology) domains.,tissue specificity:Highly expressed in brain, kidney, pancreas, and liver, and at lower levels in lung and placenta.,
  • 相關(guān)產(chǎn)品: RS0001,RS0002,YM3028,YM3029
  • 細(xì)胞定位: Cytoplasm, cytoskeleton. Cytoplasm, cell cortex.
  • 組織表達(dá): Highly expressed in brain, kidney, pancreas, and liver, and at lower levels in lung and placenta.
  • 科研貨號: PLA020768
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.zjgzfxx.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
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