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C5 anticorps (AA 1-77)

Cet anticorps Lapin Polyclonal détecte spécifiquement C5 dans WB et IHC. Il présente une réactivité envers Rat.
N° du produit ABIN3043765

Aperçu rapide pour C5 anticorps (AA 1-77) (ABIN3043765)

Antigène

Voir toutes C5 Anticorps
C5 (Complement Component 5 (C5))

Reactivité

  • 125
  • 33
  • 22
  • 16
  • 2
  • 2
  • 2
Rat

Hôte

  • 113
  • 22
  • 4
  • 3
Lapin

Clonalité

  • 121
  • 21
Polyclonal

Conjugué

  • 56
  • 13
  • 12
  • 8
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp C5 est non-conjugé

Application

  • 76
  • 50
  • 44
  • 39
  • 34
  • 18
  • 13
  • 11
  • 11
  • 10
  • 7
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Épitope

    • 21
    • 15
    • 15
    • 12
    • 11
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-77

    Fonction

    Anti-C5/C5a Antibody Picoband®

    Réactivité croisée (Details)

    No cross-reactivity with other proteins

    Attributs du produit

    Rabbit IgG polyclonal antibody for Complement C5(C5) detection. Tested with WB, IHC-P in Rat.
    Gene Name: complement component 5
    Protein Name: Complement C5

    Purification

    Immunogen affinity purified.

    Immunogène

    E.coli-derived rat C5a recombinant protein (Position: D1-R77). Rat C5a shares 62% and 82% amino acid (aa) sequences identity with human and mouse C5a, respectively.

    Isotype

    IgG
  • Indications d'application

    Immunohistochemistry (Paraffin-embedded Section), 0.5-1 μg/mL, Rat
    Western blot, 0.1-0.5 μg/mL, Rat
    1. Delgado-Cervino, E., Fontan, G., Lopez-Trascara, M. C5 complement deficiency in a Spanish family: molecular characterization of the double mutation responsible for the defect. Molec. Immun. 42: 105-111, 2005. 2. Pfarr, N., Prawitt, D., Kirschfink, M., Schroff, C., Knuf, M., Habermehl, P., Mannhardt, W., Zepp, F., Fairbrother, W. G., Loos, M., Burge, C. B., Pohlenz, J. Linking C5 deficiency to an exonic splicer enhancer mutation. J. Immun. 174: 4172-4177, 2005. Note: Erratum: J. Immun. 182: 5152 only, 2009.

    Commentaires

    Antibody can be supported by chemiluminescence kit ABIN921124 in WB, supported by ABIN921231 in IHC(P).

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg 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

    4 °C,-20 °C

    Stockage commentaire

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
  • Antigène

    C5 (Complement Component 5 (C5))

    Autre désignation

    C5

    Sujet

    Synonyms: Complement C5,C5a anaphylatoxin,C5,

    Tissue Specificity: Expressed in normal hepatocytes as well as in epithelial cells lining the stomach, the small and the large intestine. Found also in basal keratinocytes of esophagus and skin. High levels are found in liver, gastrointestinal tract, thyroid and kidney. Also present in the brain. .

    Background: C5a is a protein fragment released from complement component C5. This gene is mapped to 9q33.2. The protein encoded by this gene is the fifth component of complement, which plays an important role in inflammatory and cell killing processes. This protein is comprised of alpha and beta polypeptide chains that are linked by a disulfide bridge. An activation peptide, C5a, which is an anaphylatoxin that possesses potent spasmogenic and chemotactic activity, is derived from the alpha polypeptide via cleavage with a convertase. C5a plays a key role in increasing migration and adherence of neutrophils and monocytes to vessel walls. Mutations in this gene cause complement component 5 deficiency, a disease where patients show a propensity for severe recurrent infections. Defects in this gene have also been linked to susceptibility to liver fibrosis and to rheumatoid arthritis.

    Sequence Similarities: Belongs to the protein kinase superfamily. Tyr protein kinase family.

    Poids moléculaire

    115 kDa

    ID gène

    362119

    UniProt

    P08650

    Pathways

    Système du Complément, Carbohydrate Homeostasis
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