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S26A4 Polyclonal Antibody

CAT: 0965-JOT-AP14005-01Size: 20 µLDry Ice: NoHazardous: No
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CAT#:0965-JOT-AP14005-01Size:20 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Background
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.
CAS Number
9007-83-4
Synonyms
Pendrin ;Sodium-independent chloride/iodide transporter;Solute carrier family 26 member 4
Host
Rabbit
Reactivity
Human, Rat, Mouse
Immunogen
Synthesized peptide derived from part region of human protein
Clonality
Polyclonal
Applications
WB, ELISA
Stability
-20°C for 1 year
Concentration
1 mg/ml
Antibody Type
Primary antibody
Isotype
IgG

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