RHCE anticorps (AA 2-120)
Aperçu rapide pour RHCE anticorps (AA 2-120) (ABIN760346)
Antigène
Voir toutes RHCE AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 2-120
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Fonction
- RHCE Polyclonal Antibody
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Homologie
- Human
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Purification
- Purified by Protein A.
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Immunogène
- KLH conjugated synthetic peptide derived from human RHCE
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Isotype
- IgG
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Indications d'application
- Optimal working dilution should be determined by the investigator.
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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Agent conservateur
- ProClin
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Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.
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Date de péremption
- 12 months
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- RHCE (Rhesus Blood Group, CcEe Antigens (RHCE))
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Autre désignation
- Rhce
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Sujet
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Synonyms: Blood group RhCcEe antigen, CD240CE, CD240CE antigen, RH, Rh blood group antigen Evans, Rh blood group C antigen, Rh blood group, CcEe antigens, Rh polypeptide 1, Rh polypeptide I, RH30A, Rh4, RHC, RHCE blood group variant Crawford antigen Rh43, RHE, Rhesus blood group CE protein, Rhesus blood group E antigen, Rhesus blood group Rhce antigen, Rhesus blood group, CcEe antigens, Rhesus C/E antigens, Rhesus system C and E polypeptides, RhIVbJ, RHIXB, RHPI, RhVI, RhVIII.RHCE_HUMAN
Background: The Rh blood group system is the second most clinically significant of the blood groups, second only to ABO. It is also the most polymorphic of the blood groups, with variations due to deletions, gene conversions, and missense mutations. The Rh blood group includes this gene which encodes both the RhC and RhE antigens on a single polypeptide and a second gene which encodes the RhD protein. The classification of Rh-positive and Rh-negative individuals is determined by the presence or absence of the highly immunogenic RhD protein on the surface of erythrocytes. A mutation in this gene results in amorph-type Rh-null disease. There are thirteen named isoforms.
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ID gène
- 6006
Antigène
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