OVOL2 Antikörper (AA 90-170)
Kurzübersicht für OVOL2 Antikörper (AA 90-170) (ABIN7230428)
Target
Alle OVOL2 Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- AA 90-170
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Verwendungszweck
- OVOL2 Polyclonal Antibody
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Spezifität
- The antibody detects endogenous levels of OVOL2 protein
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Aufreinigung
- The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen
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Immunogen
- Synthesized peptide derived from part region of human OVOL2 protein at AA range: 90-170
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Isotyp
- IgG
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Applikationshinweise
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).
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Kommentare
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Primary Antibody
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 1 mg/mL
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Buffer
- PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- OVOL2 (Ovo-Like 2 (OVOL2))
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Andere Bezeichnung
- OVOL2
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Hintergrund
- Rabbit Anti-OVOL2 Polyclonal Antibody,Transcription factor Ovo-like 2, hOvo2, Zinc finger protein 339,OVOL2 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 OVOL2 have been associated with posterior polymorphous corneal dystrophy.,OVOL2
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Molekulargewicht
- observerd band 30kDa
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Gen-ID
- 58495
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UniProt
- Q9BRP0
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Pathways
- Tube Formation
Target
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