ARG63610
anti-USH1C / Harmonin antibody
anti-USH1C / Harmonin antibody for Western blot and Human
Neuroscience antibody
Overview
| Product Description | Goat Polyclonal antibody recognizes USH1C / Harmonin |
|---|---|
| Tested Reactivity | Hu |
| Predict Reactivity | Ms, Rat, Cow |
| Tested Application | WB |
| Specificity | This antibody is expected to recognize both reported isoforms (NP_005700.2 and NP_710142.1). |
| Host | Goat |
| Clonality | Polyclonal |
| Isotype | IgG |
| Target Name | USH1C / Harmonin |
| Antigen Species | Human |
| Immunogen | DRKVAREFRHKVD-C |
| Conjugation | Un-conjugated |
| Alternate Names | Harmonin; DFNB18A; PDZ-73; Protein PDZ-73; ush1cpst; PDZ-45; PDZ-73/NY-CO-38; DFNB18; Autoimmune enteropathy-related antigen AIE-75; Antigen NY-CO-38/NY-CO-37; NY-CO-38; NY-CO-37; Usher syndrome type-1C protein; PDZ73; AIE-75; Renal carcinoma antigen NY-REN-3; PDZD7C |
Application Instructions
| Application Suggestion |
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|---|---|---|---|---|---|
| Application Note | WB: Recommend incubate at RT for 1h. * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
| Form | Liquid |
|---|---|
| Purification | Purified from goat serum by antigen affinity chromatography. |
| Buffer | Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA. |
| Preservative | 0.02% Sodium azide |
| Stabilizer | 0.5% BSA |
| Concentration | 0.5 mg/ml |
| Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
| Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
| Database Links | |
|---|---|
| Background | 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. [provided by RefSeq, Mar 2009] |
| Research Area | Neuroscience antibody |
| Calculated MW | 62 kDa |
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