ARG40168
anti-POU4F3 antibody
anti-POU4F3 antibody for Western blot and Human,Mouse
Overview
Product Description | Goat Polyclonal antibody recognizes POU4F3 |
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Tested Reactivity | Hu, Ms |
Predict Reactivity | Dog, Rat |
Tested Application | WB |
Host | Goat |
Clonality | Polyclonal |
Isotype | IgG |
Target Name | POU4F3 |
Antigen Species | Human |
Immunogen | Synthetic peptide around the internal region of Human POU4F3. (C-EAAYREKNSKPE, NP_002691.1) |
Conjugation | Un-conjugated |
Alternate Names | Brn-3C; BRN3C; Brain-3C; DFNA15; Brain-specific homeobox/POU domain protein 3C; POU domain, class 4, transcription factor 3 |
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. |
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Observed Size | ~ 40 kDa |
Properties
Form | Liquid |
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Purification | Affinity purified |
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 |
Swiss-port # Q15319 Human POU domain, class 4, transcription factor 3 Swiss-port # Q63955 Mouse POU domain, class 4, transcription factor 3 |
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Gene Symbol | POU4F3 |
Gene Full Name | POU class 4 homeobox 3 |
Background | This gene encodes a member of the POU-domain family of transcription factors. POU-domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15. [provided by RefSeq, Mar 2009] |
Function | May play a role in determining or maintaining the identities of a small subset of visual system neurons. [UniProt] |
Cellular Localization | Nucleus. Cytoplasm. Note=Preferentially localized in the nucleus. [UniProt] |
Calculated MW | 37 kDa |