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OTX2

Anti-OTX2 Products
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- Derivation: Mouse
- Species Reactivity: Human
- Type: Mouse IgG1
- Application: WB, IHC, ICC, FC, ELISA
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- Derivation: Mouse
- Species Reactivity: Human
- Type: Mouse IgG1
- Application: WB, IHC, ICC, FC, ELISA
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- Derivation: Mouse
- Species Reactivity: Human
- Type: Mouse IgG1, κ
- Application: WB
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- Species Reactivity: Human
- Type: Mouse IgG
- Application: WB, IHC, IF, ELISA
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- Species Reactivity: Human
- Type: IgG
- Application: IP, IF
- Anti-Mouse OTX2 Immunohistochemistry Kit (VS-0525-XY5122)
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- Species Reactivity: Human, Mouse, Rat
- Target: OTX2
- Application: IHC
- Anti-OTX2 Immunohistochemistry Kit (VS-0525-XY5121)
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- Species Reactivity: Human
- Target: OTX2
- Application: IHC
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- Derivation: Phage display library screening
- Species Reactivity: Human
- Type: IgG
- Application: IHC-P, WB
- Mouse Anti-OTX2 Monoclonal Antibody (VS7-0425-WR528) (VS7-0425-WR528)
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- Species Reactivity: Human
- Type: Mouse IgG
- Application: WB, IHC-P, IF, ICC, FC, ELISA
- Mouse Anti-OTX2 Monoclonal Antibody (VS7-0425-WR527) (VS7-0425-WR527)
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- Species Reactivity: Human
- Type: Mouse IgG
- Application: WB, IHC-P, IF, ICC, ELISA
- Mouse Anti-OTX2 Monoclonal Antibody (clone 1H12G8B2) (VS7-0425-WR526)
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- Species Reactivity: Human
- Type: Mouse IgG1
- Application: WB, IHC, ICC
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For Research Use Only. Not For Clinical Use.
This gene encodes a member of the bicoid subfamily of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and plays a role in brain, craniofacial, and sensory organ development. The encoded protein also influences the proliferation and differentiation of dopaminergic neuronal progenitor cells during mitosis. Mutations in this gene cause syndromic microphthalmia 5 (MCOPS5) and combined pituitary hormone deficiency 6 (CPHD6). This gene is also suspected of having an oncogenic role in medulloblastoma. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Pseudogenes of this gene are known to exist on chromosomes two and nine.