AMPD3 (Human) Recombinant Protein (Q01)-蛋白质/抗原/多肽-试剂-生物在线
AMPD3 (Human) Recombinant Protein (Q01)

AMPD3 (Human) Recombinant Protein (Q01)

商家询价

产品名称: AMPD3 (Human) Recombinant Protein (Q01)

英文名称: AMPD3 (Human) Recombinant Protein (Q01)

产品编号: H00000272-Q01

产品价格: 0

产品产地: 台湾

品牌商标: Abnova

更新时间: null

使用范围: null

亚诺法生技股份有限公司(Abnova)
  • 联系人 :
  • 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
  • 邮编 : 11493
  • 所在区域 : 台湾
  • 电话 : +886-920**1152
  • 传真 : +886-2-8751-1186
  • 邮箱 : sales@abnova.com.tw

  • Specification
  • Product Description:
  • Human AMPD3 partial ORF ( NP_000471, 2 a.a. - 82 a.a.) recombinant protein with GST-tag at N-terminal.
  • Sequence:
  • ALSSEPAEMPRQFPKLNISEVDEQVRLLAEKVFAKVLREEDSKDALSLFTVPEDCPIGQKEAKERELQKELAEQKSVETAK
  • Theoretical MW (kDa):
  • 34.65
  • Purification:
  • Glutathione Sepharose 4 Fast Flow
  • Storage Buffer:
  • 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Quality Control Testing:
  • 12.5% SDS-PAGE Stained with Coomassie Blue.

    QC Testing of H00000272-Q01
  • Note:
  • Best use within three months from the date of receipt of this protein.
  • Applications
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Application Image
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Gene Information
  • Entrez GeneID:
  • 272
  • Gene Name:
  • AMPD3
  • Gene Alias:
  • -
  • Gene Description:
  • adenosine monophosphate deaminase (isoform E)
  • Gene Summary:
  • 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
  • Other Designations:
  • AMP aminohydrolase,AMP deaminase 3,adenosine monophosphate deaminase 3,erythrocyte type AMP deaminase,erythrocyte-specific AMP deaminase,myoadenylate deaminase
  • Related Disease

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