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S26A4 Polyclonal Antibody

CAT: 1027-RA34657-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:1027-RA34657-01Size:50 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Background
Solute carrier family 26 member 4 (SLC26A4) Homo sapiens 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]
Gene ID
5172
Swiss Prot
O43511
Cross Reactivity
Human; Rat; Mouse
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Buffer
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Molecular Weight
85
Storage Conditions
-20°C/1 year
Protein Weight
85

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