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Recombinant Human SLC26A5, GST-tagged

Cat.No. : SLC26A5-112H
Product Overview : Recombinant Human SLC26A5(1 a.a. - 447 a.a.), fused with GST-tag at N-terminal, was expressed in wheat germ.
  • Specification
  • Gene Information
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Description : This gene encodes a member of the SLC26A/SulP transporter family. The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea, inducing changes in cell length that act to amplify sound levels. The transmembrane protein is an incomplete anion transporter, and does not allow anions to cross the cell membrane but instead undergoes a conformational change in response to changes in intracellular Cl- levels that results in a change in cell length. The protein functions at microsecond rates, which is several orders of magnitude faster than conventional molecular motor proteins. Mutations in this gene are potential candidates for causing neurosensory deafness. Multiple transcript variants encoding different isoforms have been found for this gene.
Source : Wheat germ
Species : Human
Tag : GST
Molecular Mass : 75 kDa
AA Sequence : MDHAEENEILAATQRYYVERPIFSH PVLQERLHTKDKVPDSIADKLKQAF TCTPKKIRNIIYMFLPITKWLPAYK FKEYVLGDLVSGISTGVLQLPQGLA FAMLAAVPPIFGLYSSFYPVIMYCF LGTSRHISIGPFAVISLMIGGVAVR LVPDDIVIPGGVNATNGTEARDALR VKVAMSVTLLSGIIQFCLGVCRFGF VAIYLTEPLVRGFTTAAAVHVFTSM LKYLFGVKTKRYSGIFSVVYSTVAV LQNVKNLNVCSLGVGLMVFGLLLGG KEFNERFKEKLPAPIPLEFFAVVMG TGISAGFNLKESYNVDVVGTLPLGL LPPANPDTSLFHLVYVDAIAIAIVG FSVTISMAKTLANKHGYQVDGNQEL IALGLCNSIGSLFQTFSISCSLSRS LVQEGTGGKTQTIWLTTFVSSLFLG LDYGLITAVIIALLTVIYRTQR
Applications : ELISA; WB-Re; AP; Array
Notes : Best use within three months from the date of receipt of this protein.
Storage : Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Storage Buffer : 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Gene Name : SLC26A5 solute carrier family 26 (anion exchanger), member 5 [ Homo sapiens (human) ]
Official Symbol : SLC26A5
Synonyms : SLC26A5; solute carrier family 26, member 5 (prestin); PRES, prestin (motor protein); prestin; deafness; neurosensory; autosomal recessive; 61; DFNB61; prestin (motor protein); PRES; MGC118886; MGC118887; MGC118888; MGC118889
Gene ID : 375611
mRNA Refseq : NM_001167962
Protein Refseq : NP_001161434
MIM : 604943
UniProt ID : P58743
Chromosome Location : 7q22.1
Function : secondary active sulfate transmembrane transporter activity; spectrin binding

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For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.

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