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