OVOL2 Antikörper
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- Target Alle OVOL2 Antikörper anzeigen
- OVOL2 (Ovo-Like 2 (OVOL2))
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Reaktivität
- Human, Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser OVOL2 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Antigen affinity purification
- Immunogen
- Fusion protein of human OVOL2
- Isotyp
- IgG
- Top Product
- Discover our top product OVOL2 Primärantikörper
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- Applikationshinweise
- WB 1:500-1:2000, IHC 1:30-1:150, ELISA 1:5000-1:10000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 0.84 mg/mL
- Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, 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
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- OVOL2 (Ovo-Like 2 (OVOL2))
- Andere Bezeichnung
- OVOL2 (OVOL2 Produkte)
- Synonyme
- znf339 antikoerper, MGC89597 antikoerper, EUROIMAGE566589 antikoerper, ZNF339 antikoerper, 1700108N11Rik antikoerper, 1810007D21Rik antikoerper, M-OVO antikoerper, M-OVO-A antikoerper, M-OVO-B antikoerper, MOVO antikoerper, Ovo2 antikoerper, Zfp339 antikoerper, movo2 antikoerper, ovo like zinc finger 2 antikoerper, ovo-like zinc finger 2 antikoerper, OVOL2 antikoerper, ovol2 antikoerper, Ovol2 antikoerper
- Hintergrund
- This gene encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intrinsically disordered domains. Members of this family are involved in epithelial development and differentiation. Knockout of this gene in mouse results in early embryonic lethality with phenotypes that include neurectoderm expansion, impaired vascularization, and heart anomalies. In humans, allelic variants of this gene have been associated with posterior polymorphous corneal dystrophy.
- Molekulargewicht
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Observed_MW: Refer to figures
Calculated_MW: 30 kDa
- UniProt
- Q9BRP0
- Pathways
- Tube Formation
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