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MCCC2 anticorps (C-Term)

L’anticorps Lapin Polyclonal anti-MCCC2 a été validé pour WB. Il convient pour détecter MCCC2 dans des échantillons de Humain.
N° du produit ABIN1537373

Aperçu rapide pour MCCC2 anticorps (C-Term) (ABIN1537373)

Antigène

Voir toutes MCCC2 Anticorps
MCCC2 (Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))

Reactivité

  • 43
  • 20
  • 7
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 39
  • 6
Lapin

Clonalité

  • 43
  • 2
Polyclonal

Conjugué

  • 30
  • 6
  • 3
  • 2
  • 2
  • 2
Cet anticorp MCCC2 est non-conjugé

Application

  • 45
  • 19
  • 12
  • 6
  • 6
  • 5
  • 4
  • 4
  • 1
Western Blotting (WB)

Clone

RB39210
  • Épitope

    • 8
    • 7
    • 6
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 468-496, C-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This MCCC2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 468-496 amino acids from the C-terminal region of human MCCC2.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    MCCC2 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Date de péremption

    6 months
  • Antigène

    MCCC2 (Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))

    Autre désignation

    MCCC2

    Sujet

    This gene encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism.

    Poids moléculaire

    61333

    ID gène

    64087

    NCBI Accession

    NP_071415

    UniProt

    Q9HCC0
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