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SGSH Rabbit mAb
商品货号: PRM8246
适 应 性: Human
WB IHC IF ICC
¥800元
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商品描述
  • 发货日期: 现货
  • 靶点-Target: SGSH
  • 反应性-Reactivity: Human
  • 应用-Applications: WB,IHC,IF,ICC
  • MW(Observed): 55kD
  • 宿主物种-Host Species: Rabbit
  • 同种型-Isotype: IgG,Kappa
  • 偶联-Conjugate: Unmodified
  • 推荐稀释比: WB 1:1000-5000;IHC 1:100-300;ICC/IF 1:100-300
  • 组成: PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
  • 纯化工艺: Protein A
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 克隆性: Monoclonal
  • 克隆号: PT0814R
  • 特异性: Endogenous
  • 基因名称: SGSH;HSS
  • 蛋白名称: N-sulphoglucosamine sulphohydrolase;Sulfoglucosamine sulfamidase;Sulphamidase;
  • 别名: SGSH;HSS;N-sulphoglucosamine sulphohydrolase ;Sulfoglucosamine sulfamidase;Sulphamidase;
  • Organism-1: Human
  • 基因ID-1: 6448
  • SwissProt-1: P51688
  • 背景: This gene encodes the enzyme sulfamidase; one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with the lysosomal storage disease mucopolysaccaridosis IIIA, also known as Sanfilippo syndrome A, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined. [provided by RefSeq, Jun 2017]
  • 细胞定位: Lysosome.
SGSH Rabbit mAb
Catalog No PRM8246
Product information
  • 发货日期: 现货
  • 靶点-Target: SGSH
  • 反应性-Reactivity: Human
  • 应用-Applications: WB,IHC,IF,ICC
  • MW(Observed): 55kD
  • 宿主物种-Host Species: Rabbit
  • 同种型-Isotype: IgG,Kappa
  • 偶联-Conjugate: Unmodified
  • 推荐稀释比: WB 1:1000-5000;IHC 1:100-300;ICC/IF 1:100-300
  • 组成: PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
  • 纯化工艺: Protein A
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 克隆性: Monoclonal
  • 克隆号: PT0814R
  • 特异性: Endogenous
  • 基因名称: SGSH;HSS
  • 蛋白名称: N-sulphoglucosamine sulphohydrolase;Sulfoglucosamine sulfamidase;Sulphamidase;
  • 别名: SGSH;HSS;N-sulphoglucosamine sulphohydrolase ;Sulfoglucosamine sulfamidase;Sulphamidase;
  • Organism-1: Human
  • 基因ID-1: 6448
  • SwissProt-1: P51688
  • 背景: This gene encodes the enzyme sulfamidase; one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with the lysosomal storage disease mucopolysaccaridosis IIIA, also known as Sanfilippo syndrome A, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined. [provided by RefSeq, Jun 2017]
  • 细胞定位: Lysosome.
  • Hunan UPT Biotechnology Co.,Ltd
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    E-mail:service@uptbio.com
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