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ACY2 rabbit pAb
商品货号: PLA009554
适 应 性: 人,小鼠,大鼠
WB
¥600元
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MSDS
说明书
商品描述
  • 发货日期: 7
  • 基因名称: ASPA ACY2 ASP
  • 蛋白名称: ACY2
  • Human_gene_id: 443
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=443
  • Human_swiss_prot_no: P45381
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P45381/entry
  • Mouse_gene_id: 11484
  • Mouse_gene_link: https://www.uniprot.org/uniprot/11484
  • Mouse_swiss_prot_no: Q8R3P0
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q8R3P0
  • Rat_gene_id: 79251
  • Rat_gene_link: https://www.uniprot.org/uniprot/79251
  • Rat_swiss_prot_no: Q9R1T5
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/Q9R1T5
  • 特异性: This antibody detects endogenous levels of ACY2 at Human/Mouse/Rat
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 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
  • 分子量: 34kD
  • 功能: catalytic activity:N-acyl-L-aspartate + H(2)O = a carboxylate + L-aspartate.,cofactor:Binds 1 zinc ion per subunit.,disease:Defects in ASPA are the cause of Canavan disease (CAND) [MIM:271900]; also known as spongy degeneration of the brain. CAND is a rare neurodegenerative condition of infancy or childhood characterized by white matter vacuolization and demeylination that gives rise to a spongy appearance. The clinical features are onset in early infancy, atonia of neck muscles, hypotonia, hyperextension of legs and flexion of arms, blindness, severe mental defect, megalocephaly, and death by 18 months on the average.,function:Catalyzes the deacetylation of N-acetylaspartic acid (NAA) to produce acetate and L-aspartate. NAA occurs in high concentration in brain and its hydrolysis NAA plays a significant part in the maintenance of intact white matter. In other tissues it act as a scavenger of NAA from body fluids.,similarity:Belongs to the aspA/astE family. Aspartoacylase subfamily.,subunit:Homodimer.,tissue specificity:Brain white matter, skeletal muscle, kidney, adrenal glands, lung and liver.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Cytoplasm. Nucleus .
  • 组织表达: Brain white matter, skeletal muscle, kidney, adrenal glands, lung and liver.
  • 科研货号: PLA009554
ACY2 rabbit pAb
Catalog No PLA009554
Product information
  • 发货日期: 7
  • 基因名称: ASPA ACY2 ASP
  • 蛋白名称: ACY2
  • Human_gene_id: 443
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=443
  • Human_swiss_prot_no: P45381
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P45381/entry
  • Mouse_gene_id: 11484
  • Mouse_gene_link: https://www.uniprot.org/uniprot/11484
  • Mouse_swiss_prot_no: Q8R3P0
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q8R3P0
  • Rat_gene_id: 79251
  • Rat_gene_link: https://www.uniprot.org/uniprot/79251
  • Rat_swiss_prot_no: Q9R1T5
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/Q9R1T5
  • 特异性: This antibody detects endogenous levels of ACY2 at Human/Mouse/Rat
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 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
  • 分子量: 34kD
  • 功能: catalytic activity:N-acyl-L-aspartate + H(2)O = a carboxylate + L-aspartate.,cofactor:Binds 1 zinc ion per subunit.,disease:Defects in ASPA are the cause of Canavan disease (CAND) [MIM:271900]; also known as spongy degeneration of the brain. CAND is a rare neurodegenerative condition of infancy or childhood characterized by white matter vacuolization and demeylination that gives rise to a spongy appearance. The clinical features are onset in early infancy, atonia of neck muscles, hypotonia, hyperextension of legs and flexion of arms, blindness, severe mental defect, megalocephaly, and death by 18 months on the average.,function:Catalyzes the deacetylation of N-acetylaspartic acid (NAA) to produce acetate and L-aspartate. NAA occurs in high concentration in brain and its hydrolysis NAA plays a significant part in the maintenance of intact white matter. In other tissues it act as a scavenger of NAA from body fluids.,similarity:Belongs to the aspA/astE family. Aspartoacylase subfamily.,subunit:Homodimer.,tissue specificity:Brain white matter, skeletal muscle, kidney, adrenal glands, lung and liver.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Cytoplasm. Nucleus .
  • 组织表达: Brain white matter, skeletal muscle, kidney, adrenal glands, lung and liver.
  • 科研货号: PLA009554
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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