USH1C antibody
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935106861
info@markelab.com
name
USH1C antibody
category
Primary Antibodies
provider
FineTest
reference
FNab03757
tested applications
ELISA, WB, IHC
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Usher syndrome 1C(autosomal recessive, severe) (USH1C) |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Recommended Dilution | WB: 1:500-1:2000; IHC: 1:20-1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 68-73 kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, WB, IHC |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.) |
| UniProt ID | Q9Y6N9 |
| Alias | Harmonin,Antigen NY-CO-38/NY-CO-37,Autoimmune enteropathy-related antigen AIE-75,Protein PDZ-73,Renal carcinoma antigen NY-REN-3,Usher syndrome type-1C protein,USH1C,AIE75 |
| Background | Antibody anti-USH1C |
| Status | RUO |
| Note | Mol. Weight 68-73 kDa |
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USH1C Antibody is a Rabbit Polyclonal antibody against USH1C. This 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.
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