DFNB31 Antibody
Product Specifications
Background
This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.
NCBI Gene ID
25861
Swiss Prot
Q9P202
Accession Number
Q9P202
Host
Rabbit
Reactivity
Human
Immunogen
This DFNB31 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 378-406 amino acids from the Central region of human DFNB31.
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Neuroscience
Purification
This antibody is purified through a protein A column, followed by peptide affinity purification.
Concentration
Batch dependent
Buffer
Supplied in PBS with 0.09% (W/V) sodium azide.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at 4˚ C for three months and -20˚ C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Product Datasheet
https://www.prosci-inc.com/?datasheet_sku=55-639
Calculated Molecular Weight
97 kDa
Fragment
Rabbit Ig
Symbol
DFNB31
NCBI Official Name
Whirlin
NCBI Organism
Homo sapiens
Background Reference 01
Letra, A., et al. Am. J. Med. Genet.152A (7), 1701-1710 (2010) :
Background Reference 02
Secolin, R., et al. Psychiatr. Genet. 20 (3) :126-129 (2010)
Background Reference 03
Aller, E., et al. Mol. Vis. 16, 495-500 (2010) :
Background Reference 04
Toiyama, Y., et al. Int. J. Oncol. 35 (4) :709-715 (2009)
Other Product Names
Whirlin, Autosomal recessive deafness type 31 protein, DFNB31, KIAA1526, WHRN
Tested Applications
WB, IHC-P
Protein ID
296453079
Physical Properties
Liquid
Curated Selection
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