Anti-ASS1 Polyclonal Antibody-一抗-抗体-蛋白与免疫

Anti-ASS1 Polyclonal Antibody

品牌:solarbio | 货号:K007276P

英文名称 Anti-ASS1 Polyclonal Antibody
宿主 Rabbit
别名 ASS;CTLN1
应用 WB
稀释比例 WB 1:500-2000.
交叉反应 Human Mouse Rat
蛋白分子量 47kDa
Gene ID 445
保存 Store at -20°C. Avoid freeze / thaw cycles.
储存液 Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
纯化方法 Affinity purification
亚型 IgG
免疫原 Recombinant protein of human ASS1
性状 液体
Public Immunogen Range Recombinant protein of human ASS1
Subcellular Locations Cytosol
Swiss Prot P00966
克隆类型 Polyclonal Antibody
背景资料 The protein encoded by this gene catalyzes the penultimate step of the arginine biosynthetic pathway. There are approximately 10 to 14 copies of this gene including the pseudogenes scattered across the human genome, among which the one located on chromosome 9 appears to be the only functional gene for argininosuccinate synthetase. Mutations in the chromosome 9 copy of this gene cause citrullinemia. Two transcript variants encoding the same protein have been found for this gene.

Anti-UMPS Polyclonal Antibody-一抗-抗体-蛋白与免疫

Anti-UMPS Polyclonal Antibody

品牌:solarbio | 货号:K007274P

英文名称 Anti-UMPS Polyclonal Antibody
宿主 Rabbit
别名 OPRT
应用 WB IHC
稀释比例 WB 1:500-2000. IHC 1:30-150.
交叉反应 Human Mouse
蛋白分子量 52kDa
Gene ID 7372
保存 Store at -20°C. Avoid freeze / thaw cycles.
储存液 Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
纯化方法 Affinity purification
亚型 IgG
免疫原 Recombinant protein of human UMPS
性状 液体
Public Immunogen Range Recombinant protein of human UMPS
Subcellular Locations Cytoplasm Cell membrane
Swiss Prot P11172
克隆类型 Polyclonal Antibody
背景资料 This gene encodes a uridine 5′-monophosphate synthase. The encoded protein is a bifunctional enzyme that catalyzes the final two steps of the de novo pyrimidine biosynthetic pathway. The first reaction is carried out by the N-terminal enzyme orotate phosphoribosyltransferase which converts orotic acid to orotidine-5′-monophosphate. The terminal reaction is carried out by the C-terminal enzyme OMP decarboxylase which converts orotidine-5′-monophosphate to uridine monophosphate. Defects in this gene are the cause of hereditary orotic aciduria. Alternate splicing results in multiple transcript variants.?