Anti-PSMB6 Polyclonal Antibody-一抗-抗体-蛋白与免疫

Anti-PSMB6 Polyclonal Antibody

品牌:solarbio | 货号:K003745P

英文名称 Anti-PSMB6 Polyclonal Antibody
宿主 Rabbit
别名 DELTA;LMPY;Y
应用 WB IHC
稀释比例 WB 1:500-2000. IHC 1:50-200.
交叉反应 Human Mouse Rat
蛋白分子量 25kDa
Gene ID 5694
保存 Store at -20°C. Avoid freeze / thaw cycles.
储存液 Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
纯化方法 Affinity purification
亚型 IgG
免疫原 Recombinant protein of human PSMB6
性状 液体
Public Immunogen Range Recombinant protein of human PSMB6
Subcellular Locations Cytoplasm Nucleus
Swiss Prot P28072
克隆类型 Polyclonal Antibody
背景资料 The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. The encoded protein is a member of the proteasome B-type family, also known as the T1B family, and is a 20S core beta subunit in the proteasome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.

Anti-PMM2 Polyclonal Antibody-一抗-抗体-蛋白与免疫

Anti-PMM2 Polyclonal Antibody

品牌:solarbio | 货号:K003740P

英文名称 Anti-PMM2 Polyclonal Antibody
宿主 Rabbit
别名 CDG1;CDG1a;CDGS;PMI;PMI1;PMM 2
应用 WB IHC
稀释比例 WB 1:500-2000. IHC 1:50-200.
交叉反应 Human Mouse Rat
蛋白分子量 28kDa
Gene ID 5373
保存 Store at -20°C. Avoid freeze / thaw cycles.
储存液 Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
纯化方法 Affinity purification
亚型 IgG
免疫原 Recombinant protein of human PMM2
性状 液体
Public Immunogen Range Recombinant protein of human PMM2
Subcellular Locations Cytoplasm
Swiss Prot O15305
克隆类型 Polyclonal Antibody
背景资料 The protein encoded by this gene catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate, which is a precursor to GDP-mannose necessary for the synthesis of dolichol-P-oligosaccharides. Mutations in this gene have been shown to cause defects in glycoprotein biosynthesis, which manifests as carbohydrate-deficient glycoprotein syndrome type I.