Complement Factor H anticorps (Internal Region)

N° du produit ABIN372860

Détail du produit anti-Complement Factor H anticorps

Antigène: Complement Factor H (CFH)

Épitope: Internal Region

Reactivité: Humain

Hôte: Chèvre

Clonalité: Polyclonal

Conjugué: Cet anticorp Complement Factor H est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Specificité: This antibody reacts to Complement Factor H (CFH).

Purification: Immunoaffinity Chromatography

Immunogène: Synthetic peptide (C-HLVPDRKKDQYK) from an internal region of human CFH

Isotype: IgG

Information d'application

Indications d'application: Immunohistochemistry on paraffin sections: 2,5 μg/mL. Western blot: 0.03 - 0.1 μg/mL. ELISA: 1/32000.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Stockage

Buffer: Tris saline buffer, pH 7.3, 0.5 % BSA, 0.02 % sodium azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: -20 °C

Détails sur Complement Factor H

Antigène: Complement Factor H (CFH)

Abstract: CFH Produits

Synonymes: anticorps AHUS1, anticorps AMBP1, anticorps ARMD4, anticorps ARMS1, anticorps CFHL3, anticorps FH, anticorps FHL1, anticorps HF, anticorps HF1, anticorps HF2, anticorps HUS, anticorps Mud-1, anticorps NOM, anticorps Sas-1, anticorps Sas1, anticorps Fh, anticorps CFH, anticorps im:7147412, anticorps si:ch211-207o17.2, anticorps fH, anticorps armd4, anticorps arms1, anticorps cfh, anticorps cfhl3, anticorps fhl1, anticorps hf1, anticorps hf2, anticorps hus, anticorps complement factor H, anticorps complement component factor h, anticorps complement factor H-related protein 5, anticorps complement factor H L homeolog, anticorps CFH, anticorps Cfh, anticorps cfh, anticorps LOC100399888, anticorps LOC100733902, anticorps cfh.L

Sujet: The complement Factor H protein is secreted into the bloodstream and acts in the regulation of complement activation. Mutations leading to changes in this protein have been linked with HUS (hemolytic-uremic syndrome) and chronic hypocomplementemic nephropathy. Factor H is mainly synthesised in the liver but also in macrophages and endothelium. It is primarily aplasma glycoprotein but is also found in platelets and there is a membrane bound form on some leukocytes. Consisting of a single polypeptide, the major form of Factor H has a molecular weight of 155 kDa. There are two truncated forms, a non-glycosylated 49 kDa form and a glycosylated 39-43 kDaform. Plasma concentrations are in the range 200-600 mg/L for the 155 kDa form and 1-5 mg/L for thetruncated forms. Factor H is a major regulatory protein of the complement system. By binding to C3b it either displacesor prevents the binding of Bb (activated Factor B). When bound to Factor H, C3b is susceptible tocleavage by Factor 1 to yield iC3b. Factor H is released or modified following this cleavage. The regulatory role of Factor H is essential because C3bBb is not only a C5 convertase but a C3 convertaseand so has a positive feedback effect, potentially consuming the entire C3 pool if unregulated.Synonyms: CFH, H factor 1, HF, HF1, HF2

ID gène: 3075

NCBI Accession: NP_000177

UniProt: P08603

Pathways: Système du Complément, Cellular Response to Molecule of Bacterial Origin