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AMPD3 Polyclonal Antibody

说明书

BYab-02497

  • 20UL ¥460 50UL ¥945 100UL ¥1350
  • 货期: 3天左右

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宿主
反应性
应用
IHC;IF;ELISA
分子量(DA)
免疫原
Synthesized peptide derived from AMPD3 . at AA range: 280-360
特异性
AMPD3 Polyclonal Antibody detects endogenous levels of AMPD3 protein.
来源
Polyclonal, Rabbit,IgG
组成(Formulation)
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
稀释比例
IHC: 1/100 - 1/300. ELISA: 1/40000.. IF 1:50-200
纯化工艺(Immunogen)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度
1 mg/ml
背景(Background)
This gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq, Jul 2008],
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
基因名称(Gene Name)
AMPD3
蛋白名称
AMP deaminase 3
简称
AMPD3
其他名称
AMPD3; AMP deaminase 3; AMP deaminase isoform E; Erythrocyte AMP deaminase
Fields
>>Purine metabolism;>>Metabolic pathways;>>Nucleotide metabolism
人基因ID
272
人蛋白质序列数据库
Q01432
小鼠基因ID
11717
小鼠蛋白质序列数据库
O08739
大鼠基因ID
25095
大鼠蛋白质序列数据库
O09178
细胞定位
cytosol,
组织表达
Brain,Hippocampus,Keratinocyte,Synovial membrane tissue,
储存(Storage)
-20°C/1 year

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AMPD3 Polyclonal Antibody

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