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ACSF3 anticorps (AA 270-450)

Cet anticorps anti-ACSF3 est un anticorps Lapin Polyclonal détectant ACSF3 dans WB. Adapté pour Humain.
N° du produit ABIN6136454

Aperçu rapide pour ACSF3 anticorps (AA 270-450) (ABIN6136454)

Antigène

Voir toutes ACSF3 Anticorps
ACSF3 (Acyl-CoA Synthetase Family Member 3 (ACSF3))

Reactivité

  • 18
  • 10
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 16
  • 2
Lapin

Clonalité

  • 18
Polyclonal

Conjugué

  • 9
  • 3
  • 2
  • 2
  • 1
  • 1
Cet anticorp ACSF3 est non-conjugé

Application

  • 13
  • 12
  • 9
Western Blotting (WB)
  • Épitope

    • 7
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 270-450

    Séquence

    FSPQQVWEKF LSSETPRINV FMAVPTIYTK LMEYYDRHFT QPHAQDFLRA VCEEKIRLMV SGSAALPLPV LEKWKNITGH TLLERYGMTE IGMALSGPLT TAVRLPGSVG TPLPGVQVRI VSENPQREAC SYTIHAEGDE RGTKVTPGFE EKEGELLVRG PSVFREYWNK PEETKSAFTL D

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein containing a sequence corresponding to amino acids 270-450 of human ACSF3 (NP_001230208.1).

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    ACSF3 (Acyl-CoA Synthetase Family Member 3 (ACSF3))

    Autre désignation

    ACSF3

    Sujet

    This gene encodes a member of the acyl-CoA synthetase family of enzymes that activate fatty acids by catalyzing the formation of a thioester linkage between fatty acids and coenzyme A. The encoded protein is localized to mitochondria, has high specificity for malonate and methylmalonate and possesses malonyl-CoA synthetase activity. Mutations in this gene are a cause of combined malonic and methylmalonic aciduria. Alternatively spliced transcript variants have been observed for this gene.,ACSF3,Cancer,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,Hydrolysis,Lipases,Cardiovascular,Lipids,ACSF3

    Poids moléculaire

    64 kDa

    ID gène

    197322

    UniProt

    Q4G176
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