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SGSH Rabbit mAb

商品貨號(hào)： PRM8246

適應(yīng) 性： Human

￥800元

規(guī)格：

50ul

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說明書

商品描述

發(fā)貨日期：現(xiàn)貨
靶點(diǎn)-Target： SGSH
反應(yīng)性-Reactivity： Human
應(yīng)用-Applications： WB,IHC,IF,ICC
MW(Observed)： 55kD
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： WB 1:1000-5000;IHC 1:100-300;ICC/IF 1:100-300
組成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
純化工藝： Protein A
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆號(hào)： PT0814R
特異性： Endogenous
基因名稱： SGSH;HSS
蛋白名稱： N-sulphoglucosamine sulphohydrolase;Sulfoglucosamine sulfamidase;Sulphamidase;
別名： 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]
細(xì)胞定位： Lysosome.

SGSH Rabbit mAb

Catalog No PRM8246

Product information

發(fā)貨日期：現(xiàn)貨
靶點(diǎn)-Target： SGSH
反應(yīng)性-Reactivity： Human
應(yīng)用-Applications： WB,IHC,IF,ICC
MW(Observed)： 55kD
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： WB 1:1000-5000;IHC 1:100-300;ICC/IF 1:100-300
組成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
純化工藝： Protein A
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆號(hào)： PT0814R
特異性： Endogenous
基因名稱： SGSH;HSS
蛋白名稱： N-sulphoglucosamine sulphohydrolase;Sulfoglucosamine sulfamidase;Sulphamidase;
別名： 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]
細(xì)胞定位： Lysosome.