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Aminomethyltransferase antibody (N-Term)

AMT Reactivity: Human WB, FACS, IHC (p) Host: Rabbit Polyclonal RB19704 unconjugated
Catalog No. ABIN390700
  • Target See all Aminomethyltransferase (AMT) Antibodies
    Aminomethyltransferase (AMT)
    Binding Specificity
    • 6
    • 5
    • 4
    • 2
    • 1
    • 1
    AA 19-45, N-Term
    Reactivity
    • 24
    • 8
    • 7
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 20
    • 4
    Rabbit
    Clonality
    • 22
    • 2
    Polyclonal
    Conjugate
    • 20
    • 2
    • 1
    • 1
    This Aminomethyltransferase antibody is un-conjugated
    Application
    • 19
    • 8
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Predicted Reactivity
    M
    Purification
    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
    Immunogen
    This AMT antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 19-45 amino acids from the N-terminal region of human AMT.
    Clone
    RB19704
    Isotype
    Ig Fraction
    Top Product
    Discover our top product AMT Primary Antibody
  • Application Notes
    WB: 1:1000. IHC-P: 1:50~100. FC: 1:10~50
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C,-20 °C
    Storage Comment
    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
    Expiry Date
    6 months
  • Target
    Aminomethyltransferase (AMT)
    Alternative Name
    AMT (AMT Products)
    Synonyms
    F16J13.200 antibody, F16J13_200 antibody, T7P1.13 antibody, T7P1_13 antibody, wu:fc31f04 antibody, wu:fd44b12 antibody, wu:fd54h12 antibody, zgc:103483 antibody, zgc:109741 antibody, GCE antibody, GCST antibody, GCVT antibody, NKH antibody, EG434437 antibody, aminomethyltransferase antibody, Glycine cleavage T-protein family antibody, Aminomethyltransferase antibody, aminomethyltransferase L homeolog antibody, AMT antibody, AT4G12130 antibody, AT1G60990 antibody, Tb11.01.1440 antibody, Palpr_0614 antibody, Ocepr_1643 antibody, Celal_2914 antibody, Deima_1002 antibody, Deipr_1956 antibody, Bacsa_3405 antibody, Celly_0288 antibody, Weevi_0527 antibody, Fluta_3952 antibody, Marky_0785 antibody, Spico_1217 antibody, Poras_1228 antibody, Halhy_3617 antibody, amt antibody, amt.L antibody, Amt antibody
    Background
    The enzyme system for cleavage of glycine (glycine cleavage system, EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase, MIM 238300), H protein (a lipoic acid-containing protein, MIM 238330), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase, MIM 238331). Glycine encephalopathy (GCE, MIM 605899) may be due to a defect in any one of these enzymes.
    Molecular Weight
    43946
    Gene ID
    275
    NCBI Accession
    NP_000472, NP_001158182, NP_001158183, NP_001158184
    UniProt
    P48728
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