A21179
Size
  • 50ul
  • 100ul
Price
  • $129
  • $229
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Product description

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

Source
Rabbit
Applications
WB,ELISA
Reactivity
Human
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Storage
-20°C/1 year
Specificity
S26A4 Polyclonal Antibody detects endogenous levels of protein.
Source/Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Immunogen
Synthesized peptide derived from part region of human protein
Uniprot No
O43511
Form
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Clonality
Polyclonal
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
Other
Gene_name: SLC26A4 PDS ; Protein_name: Pendrin (Sodium-independent chloride/iodide transporter) (Solute carrier family 26 member 4); Expression: Thyroid,
Mol.Wt (Da)
81 kD
Concentration
1 mg/ml

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