RAG2 Antikörper (AA 46-503) (Fluoro594)
Kurzübersicht für RAG2 Antikörper (AA 46-503) (Fluoro594) (ABIN8031006)
Target
Alle RAG2 Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- AA 46-503
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Verwendungszweck
- Anti-RAG2 Antibody Fluoro594 Conjugated
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Kreuzreaktivität (Details)
- No cross-reactivity with other proteins
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Aufreinigung
- Immunogen affinity purified.
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Immunogen
- E.coli-derived human RAG2 recombinant protein (Position: F46-K503).
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Isotyp
- IgG
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Applikationshinweise
- Flow Cytometry, Optimal dilutions should be determined by end users.
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Buffer
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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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
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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Haltbarkeit
- 12 months
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- RAG2 (Recombination Activating Gene 2 (RAG2))
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Andere Bezeichnung
- RAG2
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Hintergrund
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Background: Recombination activating gene 2, also known as RAG-2, is a protein that in humans is encoded by the RAG2 gene. This gene encodes a protein that is involved in the initiation of V(D)J recombination during B and T cell development. This protein forms a complex with the product of the adjacent recombination activating gene 1, and this complex can form double-strand breaks by cleaving DNA at conserved recombination signal sequences. The recombination activating gene 1 component is thought to contain most of the catalytic activity, while the N-terminal of the recombination activating gene 2 component is thought to form a six-bladed propeller in the active core that serves as a binding scaffold for the tight association of the complex with DNA. A C-terminal plant homeodomain finger-like motif in this protein is necessary for interactions with chromatin components, specifically with histone H3 that is trimethylated at lysine 4. Mutations in this gene cause Omenn syndrome, a form of severe combined immunodeficiency associated with autoimmune-like symptoms.
Gene Full Name: recombination activating 2
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Gen-ID
- 5897
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UniProt
- P55895
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Pathways
- Chromatin Binding, Production of Molecular Mediator of Immune Response
Target
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