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PMM2 anticorps (C-Term)

L’anticorps Lapin Polyclonal anti-PMM2 a été validé pour WB. Il convient pour détecter PMM2 dans des échantillons de Humain.
N° du produit ABIN1536830

Aperçu rapide pour PMM2 anticorps (C-Term) (ABIN1536830)

Antigène

Voir toutes PMM2 Anticorps
PMM2 (Phosphomannomutase 2 (PMM2))

Reactivité

  • 30
  • 5
  • 5
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
Humain

Hôte

  • 25
  • 5
Lapin

Clonalité

  • 26
  • 3
Polyclonal

Conjugué

  • 24
  • 2
  • 1
  • 1
  • 1
  • 1
Cet anticorp PMM2 est non-conjugé

Application

  • 29
  • 17
  • 6
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

RB39495
  • Épitope

    • 9
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 198-226, C-Term

    Homologie

    B, Pr, M

    Purification

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

    Immunogène

    This PMM2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 198-226 amino acids from the C-terminal region of human PMM2.

    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

    PMM2 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

    PMM2 (Phosphomannomutase 2 (PMM2))

    Autre désignation

    PMM2

    Sujet

    The protein encoded by this gene catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate, which is a precursor to GDP-mannose necessary for the synthesis of dolichol-P-oligosaccharides. Mutations in this gene have been shown to cause defects in glycoprotein biosynthesis, which manifests as carbohydrate-deficient glycoprotein syndrome type I. [provided by RefSeq].

    Poids moléculaire

    28082

    ID gène

    5373

    NCBI Accession

    NP_000294

    UniProt

    O15305
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