OTX2 Antikörper (AA 1-204)
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- Target Alle OTX2 Antikörper anzeigen
- OTX2 (Orthodenticle Homeobox 2 (OTX2))
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Bindungsspezifität
- AA 1-204
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser OTX2 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Aufreinigung
- Protein A Chromatography
- Immunogen
- A partial length recombinant Otx2 protein (amino acids 1-204) was used as the immunogen for this antibody.
- Isotyp
- IgG
- Top Product
- Discover our top product OTX2 Primärantikörper
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- Applikationshinweise
- WB: 2-4 μg/mL
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 0.5 mg/mL
- Buffer
- PBS containing 0.05 % BSA, PH 7.4
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- 4 °C/-20 °C
- Informationen zur Lagerung
- Store the antibody at 4°C, stable for 6 months. For long-term storage, store at -20°C. Avoid repeated freeze and thaw cycles.
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- Target
- OTX2 (Orthodenticle Homeobox 2 (OTX2))
- Andere Bezeichnung
- Otx2 (OTX2 Produkte)
- Synonyme
- CPHD6 antikoerper, MCOPS5 antikoerper, E130306E05Rik antikoerper, id:ibd2915 antikoerper, zOtx2 antikoerper, zgc:136535 antikoerper, zotx-2 antikoerper, Xotx-2 antikoerper, Xotx2 antikoerper, otx-2 antikoerper, otx2 antikoerper, orthodenticle homeobox 2 antikoerper, orthodenticle homeobox 2 S homeolog antikoerper, orthodenticle homeobox 2 L homeolog antikoerper, OTX2 antikoerper, Otx2 antikoerper, otx2 antikoerper, otx2.S antikoerper, otx2.L antikoerper
- Hintergrund
- Otx2 encodes a transcription factor that plays a critical role in craniofacial development and anterior brain morphogenesis. Otx2 homologs in model organisms are expressed in a complex spatial, temporal, and gradient-specific manner that is required for correct antero-posterior patterning and craniofacial development. Otx2 mutations are associated with severe ocular phenotypes and central nervous system abnormalities such as seizures, short stature and developmental delay, CPHD (Combined Pituitary Hormone Deficiency), structural abnormalities of the pituitary gland and early onset retinal dystrophy.
- Molekulargewicht
- 32 kDa
- Gen-ID
- 5015
- UniProt
- P32243
- Pathways
- Dopaminergic Neurogenesis
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