SLC26A4 (Human) Recombinant Protein (Q01)
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More Files
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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
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
34.65
Interspecies Antigen Sequence
Mouse (83); Rat (88)
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Quality Control Testing
12.5% SDS-PAGE Stained with Coomassie Blue.
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.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Enzyme-linked Immunoabsorbent Assay
Western Blot (Recombinant protein)
Antibody Production
Protein Array
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Gene Info — SLC26A4
Entrez GeneID
5172GeneBank Accession#
NM_000441Protein Accession#
NP_000432Gene Name
SLC26A4
Gene Alias
DFNB4, EVA, PDS
Gene Description
solute carrier family 26, member 4
Gene Ontology
HyperlinkGene 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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Interactome
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Disease
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