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

GCSH anticorps (AA 1-173)

GCSH Reactivité: Humain WB, IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6141032
  • Antigène Voir toutes GCSH Anticorps
    GCSH (Glycine Cleavage System H Protein (GCSH))
    Épitope
    • 15
    • 8
    • 7
    • 6
    • 2
    • 2
    AA 1-173
    Reactivité
    • 43
    • 11
    • 11
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 41
    • 2
    Lapin
    Clonalité
    • 42
    • 1
    Polyclonal
    Conjugué
    • 12
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp GCSH est non-conjugé
    Application
    • 35
    • 19
    • 13
    • 13
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Séquence
    MALRVVRSVR ALLCTLRAVP SPAAPCPPRP WQLGVGAVRT LRTGPALLSV RKFTEKHEWV TTENGIGTVG ISNFAQEALG DVVYCSLPEV GTKLNKQDEF GALESVKAAS ELYSPLSGEV TEINEALAEN PGLVNKSCYE DGWLIKMTLS NPSELDELMS EEAYEKYIKS IEE
     Réactivité croisée
    Humain, Souris, Rat
    Attributs du produit
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-173 of human GCSH (NP_004474.2).
    Isotype
    IgG
    Top Product
    Discover our top product GCSH Anticorps primaire
  • Indications d'application
    WB,1:500 - 1:2000,IF,1:50 - 1:200
    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
    GCSH (Glycine Cleavage System H Protein (GCSH))
    Autre désignation
    GCSH (GCSH Produits)
    Synonymes
    anticorps GCE, anticorps NKH, anticorps GCSH, anticorps H-PROTEIN, anticorps 1100001L02Rik, anticorps 5730591C18Rik, anticorps wu:fb14d10, anticorps wu:fw84b08, anticorps zgc:112535, anticorps BA5228, anticorps gce, anticorps gcsh, anticorps nkh, anticorps wu:fd56h06, anticorps zgc:110557, anticorps zgc:92732, anticorps glycine cleavage system protein H, anticorps glycine cleavage system protein H (aminomethyl carrier), anticorps glycine cleavage system lipoyl carrier protein GcvH, anticorps glycine cleavage system H protein, anticorps glycine cleavage system protein H (aminomethyl carrier), a, anticorps glycine cleavage system carrier of aminomethyl moiety GcvH, anticorps leucine rich repeat containing 34, anticorps glycine cleavage system protein H (aminomethyl carrier) L homeolog, anticorps glycine cleavage system protein H (aminomethyl carrier), b, anticorps GCSH, anticorps Gcsh, anticorps gcvH-2, anticorps gcvH, anticorps gcsha, anticorps LRRC34, anticorps gcsh.L, anticorps gcshb
    Sujet
    Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the H protein, which transfers the methylamine group of glycine from the P protein to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH). Two transcript variants, one protein-coding and the other probably not protein-coding,have been found for this gene. Also, several transcribed and non-transcribed pseudogenes of this gene exist throughout the genome.,GCSH,GCE,NKH,Cancer,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,GCSH
    Poids moléculaire
    18 kDa
    ID gène
    2653
    UniProt
    P23434
Vous êtes ici:
Support technique