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Invitrogen™ DFNB31 Monoclonal Antibody (2D12)

Mouse Monoclonal Antibody

Supplier:  Invitrogen™ MA524547

Catalog No. PIMA524547


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Description

Description

Peptide Sequence: 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
Monoclonal
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
Mouse
Protein A
RUO
25861
-20°C, Avoid Freeze/Thaw Cycles
Liquid
ELISA, Immunocytochemistry
2D12
PBS with no preservative; pH 7.4
Q9P202
WHRN
DFNB31 (NP_056219, 808 a.a. ~ 907 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
100 μg
Primary
Human
Antibody
IgG1 κ
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