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 |
|
||||
---|---|---|---|---|---|
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 |
Images (1) Click the Picture to Zoom In