Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

Complement Factor H anticorps (AA 527-588)

Cet anticorps anti-Complement Factor H est un anticorps Lapin Polyclonal détectant Complement Factor H dans WB. Adapté pour Humain.
N° du produit ABIN1886532

Aperçu rapide pour Complement Factor H anticorps (AA 527-588) (ABIN1886532)

Antigène

Voir toutes Complement Factor H (CFH) Anticorps
Complement Factor H (CFH)

Reactivité

  • 68
  • 12
  • 12
  • 2
  • 2
Humain

Hôte

  • 53
  • 27
  • 3
  • 2
Lapin

Clonalité

  • 49
  • 35
  • 1
Polyclonal

Conjugué

  • 53
  • 9
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Cet anticorp Complement Factor H est non-conjugé

Application

  • 61
  • 33
  • 26
  • 22
  • 17
  • 15
  • 13
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 9
    • 6
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 527-588

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    527 - 588 of Human Complement factor H
  • Indications d'application

    Suggested dilutions:
    Western blotting: 1.500-1.3000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    1 x PBS, 1 % BSA, 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Agent conservateur

    Thimerosal (Merthiolate)

    Précaution d'utilisation

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Antigène

    Complement Factor H (CFH)

    Autre désignation

    Complement factor H

    Sujet

    This gene is a member of the Regulator of Complement Activation (RCA) gene cluster and encodes a protein with twenty short concensus 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.[provided by RefSeq]

    Poids moléculaire

    139 kDa

    ID gène

    3075

    NCBI Accession

    NP_000177, NM_000186

    Pathways

    Système du Complément, Cellular Response to Molecule of Bacterial Origin
Vous êtes ici:
Chat with us!