Learn More
DFNB31 Polyclonal Antibody, Invitrogen™
Rabbit Polyclonal Antibody
Supplier: Thermo Scientific PA5116523

Description
Positive Samples: U-87MG, HeLa, K-562, Mouse liver Immunogen sequence: PSGHPDQTGT NQHFVMVEVH RPDSEPDVNE VRALPQTRTA STLSQLSDSG QTLSEDSGVD AGEAEASAPG RGRQSVSTKS RSSKELPRNE RPTDGANKPP GLLEPTSTLV RVKKSAATLG IAIEGGANTR QPLPRIVTIQ RGGSAHNCGQ LKVGHVILEV NGLTLRGKEH REAARIIAEA FKTKDRDYID FLVTEFNVML
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.
Specifications
DFNB31 | |
Polyclonal | |
Unconjugated | |
WHRN | |
1110035G07Rik; autosomal recessive deafness type 31 protein; AW122018; AW742671; C430046P22Rik; CASK-interacting protein CIP98; CIP98; deafness, autosomal recessive 31; Dfnb31; KIAA1526; PDZD7B; USH2D; whirler; whirlin; Whrn; wi | |
Rabbit | |
Affinity chromatography | |
RUO | |
25861, 73750 | |
-20° C, Avoid Freeze/Thaw Cycles | |
Liquid |
Western Blot | |
0.92 mg/mL | |
PBS with 50% glycerol and 0.01% thimerosal; pH 7.3 | |
Q80VW5, Q9P202 | |
WHRN | |
Recombinant fusion protein containing a sequence corresponding to amino acids 708-907 of human WHRN (NP_0562193) | |
100 μL | |
Primary | |
Human, Mouse | |
Antibody | |
IgG |
Product Suggestions
Customers who viewed this item also viewed
Your input is important to us. Please complete this form to provide feedback related to the content on this product.