Thermo Fisher Scientific USH1C Polyclonal Antibody
Thermo Fisher Scientific의 USH1C 폴리클로날 항체는 인간 및 랫트 반응성을 가지며, Western blot과 IHC(Paraffin)에 적합합니다. 항원 친화 크로마토그래피로 정제된 액상 형태로 제공되며, 안정적 보관 및 재현성 높은 결과를 제공합니다.
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Thermo Fisher Scientific USH1C Polyclonal Antibody
Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 0.1–0.3 µg/mL |
| Immunohistochemistry (Paraffin) (IHC (P)) | 10 µg/mL |
Publications
- [References not provided]
Product Specifications
| Specification | Detail |
|---|---|
| Species Reactivity | Human, Rat |
| Host / Isotype | Goat / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Synthetic peptide DRKVAREFRHKVD, corresponding to N-terminal amino acids 2–14 of Human USH1C |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.5 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | TBS, pH 7.3, with 0.5% BSA |
| Contains | 0.02% sodium azide |
| Storage Conditions | Store at 4°C short term. For long-term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping Conditions | Wet ice |
| RRID | AB_2214152 |
Product Specific Information
Recommended positive controls: The peptide used to generate this antibody is available for purchase (GTX19045-PEP).
Target Information
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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