Full Product Name
S26A4 Polyclonal Antibody
Product Synonym Names
Pendrin; Sodium-independent chloride/iodide transporter; Solute carrier family 26 member 4; SLC26A4; PDS
Product Gene Name
anti-S26A4 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for O43511
Purity/Purification
Affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Form/Format
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Preparation and Storage
Store at-20 degree C for 1 year.
Other Notes
Small volumes of anti-S26A4 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Applications Tested/Suitable for anti-S26A4 antibody
Western Blot (WB), ELISA (EIA)
Application Notes for anti-S26A4 antibody
WB: 1:500-2000
ELISA: 1:5000-20000
NCBI/Uniprot data below describe general gene information for S26A4. It may not necessarily be applicable to this product.
NCBI Accession #
NP_000432.1
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NCBI GenBank Nucleotide #
NM_000441.1
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UniProt Primary Accession #
O43511
[Other Products]
UniProt Secondary Accession #
O43170; B7Z266[Other Products]
UniProt Related Accession #
O43511[Other Products]
NCBI Official Full Name
pendrin
NCBI Official Synonym Full Names
solute carrier family 26 member 4
NCBI Official Symbol
SLC26A4 [Similar Products]
NCBI Official Synonym Symbols
EVA; PDS; DFNB4; TDH2B
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NCBI Protein Information
pendrin
UniProt Protein Name
Pendrin
UniProt Synonym Protein Names
Sodium-independent chloride/iodide transporter; Solute carrier family 26 member 4
UniProt Gene Name
SLC26A4 [Similar Products]
UniProt Synonym Gene Names
PDS [Similar Products]
NCBI Summary for S26A4
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]
UniProt Comments for S26A4
Sodium-independent transporter of chloride and iodide.
Research Articles on S26A4
1. A mutation allele of GJB2 was relatively lower in the profound Chinese nonsyndromic sensorineural hearing loss population in comparison to the moderate-to-profound ones, and the c.1174A>T mutation allele of SLC26A4 was relatively higher.">Compared with previous studies, we found that the c.109G>A mutation allele of GJB2 was relatively lower in the profound Chinese nonsyndromic sensorineural hearing loss population in comparison to the moderate-to-profound ones, and the c.1174A>T mutation allele of SLC26A4 was relatively higher.
Precautions
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Disclaimer
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