Complement Factor H Antikörper
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- Target Alle Complement Factor H (CFH) Antikörper anzeigen
- Complement Factor H (CFH)
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser Complement Factor H Antikörper ist unkonjugiert
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Applikation
- Immunohistochemistry (IHC)
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human CFH (NP_001014975.1).
- Isotyp
- IgG
- Top Product
- Discover our top product CFH Primärantikörper
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- Applikationshinweise
- IHC 1:50-1:200
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- Complement Factor H (CFH)
- Andere Bezeichnung
- CFH (CFH Produkte)
- Synonyme
- AHUS1 antikoerper, AMBP1 antikoerper, ARMD4 antikoerper, ARMS1 antikoerper, CFHL3 antikoerper, FH antikoerper, FHL1 antikoerper, HF antikoerper, HF1 antikoerper, HF2 antikoerper, HUS antikoerper, Mud-1 antikoerper, NOM antikoerper, Sas-1 antikoerper, Sas1 antikoerper, Fh antikoerper, CFH antikoerper, im:7147412 antikoerper, si:ch211-207o17.2 antikoerper, fH antikoerper, armd4 antikoerper, arms1 antikoerper, cfh antikoerper, cfhl3 antikoerper, fhl1 antikoerper, hf1 antikoerper, hf2 antikoerper, hus antikoerper, complement factor H antikoerper, complement component factor h antikoerper, complement factor H-related protein 5 antikoerper, complement factor H L homeolog antikoerper, CFH antikoerper, Cfh antikoerper, cfh antikoerper, LOC100399888 antikoerper, LOC100733902 antikoerper, cfh.L antikoerper
- Hintergrund
- This gene is a member of the Regulator of Complement Activation (RCA) gene cluster and encodes a protein with twenty short consensus repeat (SCR) domains. This protein is secreted into the bloodstream and has an essential role in the regulation of complement activation, restricting this innate defense mechanism to microbial infections. Mutations in this gene have been associated with hemolytic-uremic syndrome (HUS) and chronic hypocomplementemic nephropathy. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
- Molekulargewicht
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Calculated_MW: 51kDa/139kDa
- Gen-ID
- 3075
- UniProt
- P08603
- Pathways
- Komplementsystem, Cellular Response to Molecule of Bacterial Origin
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