SLC26A4 Antibody
Product Specifications
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.
NCBI Gene ID
5172
Swiss Prot
O43511
Host
Rabbit
Reactivity
Mouse
Immunogen
A synthetic peptide corresponding to a sequence within amino acids 250-350 of human SLC26A4 (NP_000432.1) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cancer, Neuroscience, Signal Transduction
Purification
Affinity purification
Positive Control
Mouse liver
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
Observed: 86kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:2000
Symbol
SLC26A4
NCBI Official Name
Solute carrier family 26 member 4
NCBI Organism
Homo sapiens
Other Product Names
DFNB4, EVA, PDS, TDH2B, pendrin, sodium-independent chloride/iodide transporter, solute carrier family 26 (anion exchanger), member 4, truncated solute carrier family 26
Tested Applications
WB
Physical Properties
Liquid
Frequently Asked Questions
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