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

C5 anticorps (C-Term)

Cet anticorps anti-C5 est un anticorps Lapin Polyclonal détectant C5 dans WB. Adapté pour Rat.
N° du produit ABIN5518715

Aperçu rapide pour C5 anticorps (C-Term) (ABIN5518715)

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
  • 35
  • 18
  • 13
  • 11
  • 11
  • 10
  • 7
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 21
    • 15
    • 15
    • 12
    • 11
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 59-77, C-Term

    Fonction

    Anti-C5/C5a Antibody Picoband®

    Séquence

    TIADKIRKES HHKGMLLGR

    Réactivité croisée (Details)

    No cross reactivity with other proteins

    Attributs du produit

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

    Purification

    Immunogen affinity purified.

    Immunogène

    A synthetic peptide corresponding to a sequence at the C-terminus of rat C5a, different from the related mouse sequence by five amino acids.
  • Indications d'application

    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.

    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 Thimerosal, 0.05 mg Sodium azide.

    Agent conservateur

    Sodium azide, Thimerosal (Merthiolate)

    Précaution d'utilisation

    This product contains Thimerosal (Merthiolate) and Sodium azide: POISONOUS AND HAZARDOUS SUBSTANCES which should be handled by trained staff only.

    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 the testis and placenta. In the testis, restrictedly expressed in outer cell layer of seminiferous tubules. .

    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. The C5b macromolecular cleavage product can form a complex with the C6 complement component, and this complex is the basis for formation of the membrane attack complex, which includes additional complement components. 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. STE Ser/Thr protein kinase family. MAP kinase kinase subfamily.

    Poids moléculaire

    42 kDa

    ID gène

    362119

    UniProt

    P08650

    Pathways

    Système du Complément, Carbohydrate Homeostasis
Vous êtes ici:
Chat with us!