SLC26A4 (NM_000441) Human Mass Spec Standard

CAT#: PH322532

SLC26A4 MS Standard C13 and N15-labeled recombinant protein (NP_000432)



  View other "SLC26A4" proteins (3)

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CNY 14250.00


货期*
5周

规格
    • 10 ug

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Specifications

Product Data
Description SLC26A4 MS Standard C13 and N15-labeled recombinant protein (NP_000432)
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence RC222532
Predicted MW 85.5 kDa
Protein Sequence
Tag C-Myc/DDK
Purity > 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration >0.05 µg/µL as determined by microplate BCA method
Labeling Method Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine
Buffer 25 mM Tris-HCl, 100 mM glycine, pH 7.3
Reference Data
RefSeq NP_000432
RefSeq Size 4930
RefSeq ORF 2340
Synonyms DFNB4; EVA; PDS; TDH2B
Locus ID 5172
Cytogenetics 7q22.3
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, Jul 2008]
Protein Families Druggable Genome, Transmembrane
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