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AMPD3 Polyclonal Antibody
商品货号: PLA014674
适 应 性: 人,小鼠,大鼠
IHC IF ELISA
¥600元
规格:
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MSDS
说明书
商品描述
  • 基因名称: AMPD3
  • 蛋白名称: AMP deaminase 3
  • Human_gene_id: 272
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=272
  • Human_swiss_prot_no: Q01432
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/Q01432/entry
  • Mouse_gene_id: 11717
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=11717
  • Mouse_swiss_prot_no: O08739
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/O08739
  • Rat_gene_id: 25095
  • Rat_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=25095
  • Rat_swiss_prot_no: O09178
  • Rat_swiss_link: http://www.uniprot.org/uniprot/O09178
  • 特异性: AMPD3 Polyclonal Antibody detects endogenous levels of AMPD3 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 1:100 - 1:300. ELISA: 1:40000.. 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: AMPD3; AMP deaminase 3; AMP deaminase isoform E; Erythrocyte AMP deaminase
  • 分子量: 89kD
  • 信号通路: Purine metabolism;
  • 功能: catalytic activity:AMP + H(2)O = IMP + NH(3).,disease:Defects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE) [MIM:102772]. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.,function:AMP deaminase plays a critical role in energy metabolism.,pathway:Purine metabolism; IMP biosynthesis via salvage pathway; IMP from AMP: step 1/1.,similarity:Belongs to the adenosine and AMP deaminases family.,subunit:Homotetramer.,tissue specificity:Three isoforms are present in mammals: AMP deaminase 1 is the predominant form in skeletal muscle; AMP deaminase 2 predominates in smooth muscle, non-muscle tissue, embryonic muscle and undifferentiated myoblasts; AMP deaminase 3 is found in erythrocytes.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: cytosol,
  • 组织表达: Brain,Hippocampus,Keratinocyte,Synovial membrane tissue,
  • 科研货号: PLA014674
AMPD3 Polyclonal Antibody
Catalog No PLA014674
Product information
  • 基因名称: AMPD3
  • 蛋白名称: AMP deaminase 3
  • Human_gene_id: 272
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=272
  • Human_swiss_prot_no: Q01432
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/Q01432/entry
  • Mouse_gene_id: 11717
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=11717
  • Mouse_swiss_prot_no: O08739
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/O08739
  • Rat_gene_id: 25095
  • Rat_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=25095
  • Rat_swiss_prot_no: O09178
  • Rat_swiss_link: http://www.uniprot.org/uniprot/O09178
  • 特异性: AMPD3 Polyclonal Antibody detects endogenous levels of AMPD3 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 1:100 - 1:300. ELISA: 1:40000.. 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: AMPD3; AMP deaminase 3; AMP deaminase isoform E; Erythrocyte AMP deaminase
  • 分子量: 89kD
  • 信号通路: Purine metabolism;
  • 功能: catalytic activity:AMP + H(2)O = IMP + NH(3).,disease:Defects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE) [MIM:102772]. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.,function:AMP deaminase plays a critical role in energy metabolism.,pathway:Purine metabolism; IMP biosynthesis via salvage pathway; IMP from AMP: step 1/1.,similarity:Belongs to the adenosine and AMP deaminases family.,subunit:Homotetramer.,tissue specificity:Three isoforms are present in mammals: AMP deaminase 1 is the predominant form in skeletal muscle; AMP deaminase 2 predominates in smooth muscle, non-muscle tissue, embryonic muscle and undifferentiated myoblasts; AMP deaminase 3 is found in erythrocytes.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: cytosol,
  • 组织表达: Brain,Hippocampus,Keratinocyte,Synovial membrane tissue,
  • 科研货号: PLA014674
  • 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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