USH1C Mouse anti-Human, Clone: 2B3, Invitrogen
Mouse Monoclonal Antibody
Manufacturer: Invitrogen MA520917
Peptide Sequence: FTPEQIMGKD VRLLRIKKEG SLDLALEGGV DSPIGKVVVS AVYERGAAER HGGIVKGDEI MAINGKIVTD YTLAEADAAL QKAWNQGGDW IDLVVAVCPP KEYDDELTFFThis gene encodes a scaffold protein that functions in the assembly of Usher protein complexes. The protein contains PDZ domains, a coiled-coil region with a bipartite nuclear localization signal and a PEST degradation sequence. Defects in this gene are the cause of Usher syndrome type 1C and non-syndromic sensorineural deafness autosomal recessive type 18. Multiple transcript variants encoding different isoforms have been found for this gene.
|PBS with no preservative; pH 7.4|
|USH1C; harmonin; AIE-75; DFNB18; PDZ-45; PDZ-73; HARMONIN; NY-CO-37; NY-CO-38; PDZ-73/NY-CO-38; Usher syndrome 1C (autosomal recessive, severe); PDZ-73 protein; ush1cpst; deafness, autosomal recessive 18|
|-20° C, Avoid Freeze/Thaw Cycles|
|ELISA, Immunoprecipitation, Western Blot|
|USH1C (AAH16057, 424 a.a. ∽ 533 a.a) partial recombit protein with GST tag. MW of the GST tag alone is 26 KDa.|
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