C7 anticorps (AA 233-453) (Fluoro647)
Aperçu rapide pour C7 anticorps (AA 233-453) (Fluoro647) (ABIN7981446)
Antigène
Voir toutes C7 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 233-453
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Fonction
- Anti-Complement C7 Antibody Fluoro647 Conjugated
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Specificité
- No cross reactivity with other proteins.
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Réactivité croisée (Details)
- No cross-reactivity with other proteins.
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Purification
- Immunogen affinity purified.
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Immunogène
- E. coli-derived human Complement C7 recombinant protein (Position: R233-D453).
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Isotype
- IgG
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Indications d'application
- Flow Cytometry, Optimal dilutions should be determined by end users.
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Restrictions
- For Research Use only
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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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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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Date de péremption
- 12 months
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- C7 (Complement Component C7 (C7))
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Autre désignation
- C7
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Sujet
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Background: This gene encodes a serum glycoprotein that forms a membrane attack complex together with complement components C5b, C6, C8, and C9 as part of the terminal complement pathway of the innate immune system. The protein encoded by this gene contains a cholesterol-dependent cytolysin/membrane attack complex/perforin-like (CDC/MACPF) domain and belongs to a large family of structurally related molecules that form pores involved in host immunity and bacterial pathogenesis. This protein initiates membrane attack complex formation by binding the C5b-C6 subcomplex and inserts into the phospholipid bilayer, serving as a membrane anchor. Mutations in this gene are associated with a rare disorder called C7 deficiency.
Gene Full Name: complement C7
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ID gène
- 730
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UniProt
- P10643
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Pathways
- Système du Complément
Antigène
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