Arginase I Polyclonal Antibody

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商品货号： PLA014757

适应性： 人,小鼠,大鼠

￥600元

规格：

40μL 100μL 200μL

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MSDS

说明书

商品描述

基因名称： ARG1
蛋白名称： Arginase-1
Human_gene_id： 383
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=383
Human_swiss_prot_no： P05089
Human_swiss_link： http://www.uniprot.org/uniprotkb/P05089/entry
Mouse_swiss_prot_no： Q61176
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q61176
特异性： Arginase I Polyclonal Antibody detects endogenous levels of Arginase I protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： IHC-p: 100-300.WB 1:500 - 1:2000. ELISA: 1:5000.. IF 1:50-200
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： ARG1; Arginase-1; Liver-type arginase; Type I arginase
实测条带： 35kD
信号通路： Arginine and proline metabolism;
功能： catalytic activity:L-arginine + H(2)O = L-ornithine + urea.,cofactor:Binds 2 manganese ions per subunit.,disease:Defects in ARG1 are the cause of argininemia (ARGIN) [MIM:207800]; also known as hyperargininemia. Argininemia is a rare autosomal recessive disorder of the urea cycle. Arginine is elevated in the blood and cerebrospinal fluid, and periodic hyperammonemia occurs. Clinical manifestations include developmental delay, seizures, mental retardation, hypotonia, ataxia, progressive spastic quadriplegia.,induction:By arginine or homoarginine.,online information:Arginase entry,pathway:Nitrogen metabolism; urea cycle; L-ornithine and urea from L-arginine: step 1/1.,similarity:Belongs to the arginase family.,subunit:Homotrimer.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Cytoplasm . Cytoplasmic granule . Localized in azurophil granules of neutrophils (PubMed:15546957). .
组织表达： Within the immune system initially reported to be selectively expressed in granulocytes (polymorphonuclear leukocytes [PMNs]) (PubMed:15546957). Also detected in macrophages mycobacterial granulomas (PubMed:23749634). Expressed in group2 innate lymphoid cells (ILC2s) during lung disease (PubMed:27043409).
科研货号： PLA014757

Arginase I Polyclonal Antibody

Catalog No PLA014757

Product information

基因名称： ARG1
蛋白名称： Arginase-1
Human_gene_id： 383
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=383
Human_swiss_prot_no： P05089
Human_swiss_link： http://www.uniprot.org/uniprotkb/P05089/entry
Mouse_swiss_prot_no： Q61176
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q61176
特异性： Arginase I Polyclonal Antibody detects endogenous levels of Arginase I protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： IHC-p: 100-300.WB 1:500 - 1:2000. ELISA: 1:5000.. IF 1:50-200
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： ARG1; Arginase-1; Liver-type arginase; Type I arginase
实测条带： 35kD
信号通路： Arginine and proline metabolism;
功能： catalytic activity:L-arginine + H(2)O = L-ornithine + urea.,cofactor:Binds 2 manganese ions per subunit.,disease:Defects in ARG1 are the cause of argininemia (ARGIN) [MIM:207800]; also known as hyperargininemia. Argininemia is a rare autosomal recessive disorder of the urea cycle. Arginine is elevated in the blood and cerebrospinal fluid, and periodic hyperammonemia occurs. Clinical manifestations include developmental delay, seizures, mental retardation, hypotonia, ataxia, progressive spastic quadriplegia.,induction:By arginine or homoarginine.,online information:Arginase entry,pathway:Nitrogen metabolism; urea cycle; L-ornithine and urea from L-arginine: step 1/1.,similarity:Belongs to the arginase family.,subunit:Homotrimer.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Cytoplasm . Cytoplasmic granule . Localized in azurophil granules of neutrophils (PubMed:15546957). .
组织表达： Within the immune system initially reported to be selectively expressed in granulocytes (polymorphonuclear leukocytes [PMNs]) (PubMed:15546957). Also detected in macrophages mycobacterial granulomas (PubMed:23749634). Expressed in group2 innate lymphoid cells (ILC2s) during lung disease (PubMed:27043409).
科研货号： PLA014757

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