SLC26A4 Antibody

• 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