SAG Antikörper (AA 285-330)
Kurzübersicht für SAG Antikörper (AA 285-330) (ABIN1387479)
Target
Alle SAG Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- AA 285-330
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Homologie
- Human,Mouse,Rat,Dog,Cow,Sheep,Rabbit
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Aufreinigung
- Purified by Protein A.
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Immunogen
- KLH conjugated synthetic peptide derived from human Retinal S antigen
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Isotyp
- IgG
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Applikationshinweise
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 -
Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 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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Konservierungsmittel
- ProClin
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Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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Lagerung
- 4 °C,-20 °C
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Informationen zur Lagerung
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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Haltbarkeit
- 12 months
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- SAG (S-Antigen, Retina and Pineal Gland (Arrestin) (SAG))
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Andere Bezeichnung
- Retinal S antigen/S-antigen
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Hintergrund
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Synonyms: 48 kDa protein, Arrestin 1, Arrestin, ARRS_HUMAN, DKFZp686I1383, Retinal S antigen 48 KDa protein, Retinal S-antigen, Rod photoreceptor arrestin, RP47, S AG, S antigen, S antigen retina and pineal gland arrestin, S antigen retina and pineal gland, S arrestin, S-AG, S-arrestin, SAG.
Background: Plasmodium falciparum is a protozoan parasite that causes malaria. It exhibits considerable antigenic heterogeneity which may be a major problem in developing an effective vaccine against malaria. The S-antigen of Plasmodium falciparum is a highly diverse, heat stable protein that is located in the parasitophorous vacuole of the mature asexual intraerythrocytic parasite. The S-antigen gene consists of multiple alleles that originate from the same chromosome site. The amino acid sequence of each allele contains a large central section of tandemly arranged, nearly identical peptides that are specific to each allele. Thus, directed against the repeat region of a particular allele can be used to define the serotype of an S-antigen. Flanking the central repeat block are two short regions of non-repetitive sequence which occur in four different forms, each of which is utilized to define a single S-antigen family. Comparison of the four S-antigen families reveals t hat they differ considerably from each other with variation being most pronounced in the C-terminal-flanking region.
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Pathways
- Regulation of G-Protein Coupled Receptor Protein Signaling
Target
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