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OTX1 Antibody
Rabbit Polyclonal Antibody
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| WB, E |
|---|---|
| Primary Accession | P32242 |
| Reactivity | Human |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 37327 Da |
| Gene ID | 5013 |
|---|---|
| Positive Control | T47D cell line lysates |
| Application & Usage | The antibody can be used for ELISA (1:1,000) and Western blotting (1: 100~500). |
| Other Names | Orthodenticle homolg 1, Homeobox protein OTX1 |
| Target/Specificity | OTX1 |
| Antibody Form | Liquid |
| Appearance | Colorless liquid |
| Formulation | Supplied in PBS with 0.09% (W/V) sodium azide at a concentration of 0.25 mg/ml. This antibody is purified thro µgh a protein A column, followed by peptide affinity purification. |
| Handling | The antibody solution should be gently mixed before use. |
| Reconstitution & Storage | -20 °C |
| Background Descriptions | |
| Precautions | OTX1 Antibody is for research use only and not for use in diagnostic or therapeutic procedures. |
| Name | OTX1 |
|---|---|
| Function | Probably plays a role in the development of the brain and the sense organs. Can bind to the BCD target sequence (BTS): 5'-TCTAATCCC- 3'. |
| Cellular Location | Nucleus. |
| Tissue Location | Expressed in brain. Detected in the anterior part of the neural fetal retina (at protein level) |
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abcepta to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes a member of the bicoid sub-family of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and may play a role in brain and sensory organ development. A similar protein in mice is required for proper brain and sensory organ development and can cause epilepsy.
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