Invitrogen™ DFNB31 Monoclonal Antibody (2D12)

Mouse Monoclonal Antibody

Supplier:  Invitrogen™ MA524547

Catalog No. PIMA524547

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.

Specifications

• Antigen: DFNB31
• Classification: Monoclonal
• Conjugate: Unconjugated
• Gene: WHRN
• Gene Alias: 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
• Host Species: Mouse
• Purification Method: Protein A
• Regulatory Status: RUO
• Gene ID (Entrez): 25861
• Content And Storage: -20°C, Avoid Freeze/Thaw Cycles
• Form: Liquid

• Applications: ELISA, Immunocytochemistry
• Clone: 2D12
• Formulation: PBS with no preservative; pH 7.4
• Gene Accession No.: Q9P202
• Gene Symbols: WHRN
• Immunogen: DFNB31 (NP_056219, 808 a.a. ~ 907 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
• Quantity: 100 μg
• Primary or Secondary: Primary
• Target Species: Human
• Product Type: Antibody
• Isotype: IgG1 κ