SLC26A4 (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)
SLC26A4 (Human) Recombinant Protein (Q01)

SLC26A4 (Human) Recombinant Protein (Q01)

商家询价

产品名称： SLC26A4 (Human) Recombinant Protein (Q01)

英文名称： SLC26A4 (Human) Recombinant Protein (Q01)

产品编号： H00005172-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)
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进入展台

  • Specification
  • Product Description:
  • Human SLC26A4 partial ORF ( NP_000432, 674 a.a. - 754 a.a.) recombinant protein with GST-tag at N-terminal.
  • Sequence:
  • RSLRVIVKEFQRIDVNVYFASLQDYVIEKLEQCGFFDDNIRKDTFFLTVHDAILYLQNQVKSQEGQGSILETITLIQDCKD
  • 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 H00005172-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:
  • 5172
  • Gene Name:
  • SLC26A4
  • Gene Alias:
  • DFNB4,EVA,PDS
  • Gene Description:
  • solute carrier family 26, member 4
  • Gene Summary:
  • Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq
  • Other Designations:
  • pendrin

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