SPG7 (Human) Recombinant Protein (Q01)-蛋白质/抗原/多肽-试剂-生物在线
亚诺法生技股份有限公司(Abnova)
SPG7 (Human) Recombinant Protein (Q01)

SPG7 (Human) Recombinant Protein (Q01)

商家询价

产品名称: SPG7 (Human) Recombinant Protein (Q01)

英文名称: SPG7 (Human) Recombinant Protein (Q01)

产品编号: H00006687-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 点击查看
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  • 邮箱 : sales@abnova.com.tw

  • Specification
  • Product Description:
  • Human SPG7 partial ORF ( NP_003110, 655 a.a. - 754 a.a.) recombinant protein with GST-tag at N-terminal.
  • Sequence:
  • TRIAYSMVKQFGMAPGIGPISFPEAQEGLMGIGRRPFSQGLQQMMDHEARLLVAKAYRHTEKVLQDNLDKLQALANALLEKEVINYEDIEALIGPPPHGP
  • Theoretical MW (kDa):
  • 36.74
  • 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 H00006687-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:
  • 6687
  • Gene Name:
  • SPG7
  • Gene Alias:
  • CAR,CMAR,FLJ37308,MGC126331,MGC126332,PGN,SPG5C
  • Gene Description:
  • spastic paraplegia 7 (pure and complicated autosomal recessive)
  • Gene Summary:
  • This gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Two transcript variants encoding distinct isoforms have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 7. [provided by RefSeq
  • Other Designations:
  • cell adhesion regulator,cell matrix adhesion regulator,paraplegin, isoform 1,spastic paraplegia 7

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