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DFNB31 Monoclonal Antibody (2D12), Invitrogen™
Mouse Monoclonal Antibody
Brand: Invitrogen MA524547
This item is not returnable.
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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
| 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 |