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Invitrogen™ DFNB31 Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA5116523

Catalog No. PIPA5116523


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Description

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.
TRUSTED_SUSTAINABILITY
Specifications

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
ELISA, 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
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