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IHC-P analysis of human heart tissue using GTX44879 MTRR antibody at 1:600. Left to right:DAPI, MTRR, Merge. Low pH, heat-induced antigen retrieval method utilizing Sodium Citrate buffer was performed.
IHC-P analysis of human heart tissue using GTX44879 MTRR antibody at 1:600. Left to right:DAPI, MTRR, Merge. Low pH, heat-induced antigen retrieval method utilizing Sodium Citrate buffer was performed.
IHC-P analysis of human heart tissue using GTX44879 MTRR antibody at 1:600. Left to right:DAPI, MTRR, Merge. Low pH, heat-induced antigen retrieval method utilizing Sodium Citrate buffer was performed.

MTRR antibody, N-term

GTX44879
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetMTRR
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Overview

  • Supplier
    GeneTex
  • Product Name
    MTRR antibody, N-term
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 0.2-2.5 ug/ml. IHC-P: 2-10 ug/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.5-1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID4552
  • Target name
    MTRR
  • Target description
    5-methyltetrahydrofolate-homocysteine methyltransferase reductase
  • Target synonyms
    [methionine synthase]-cobalamin methyltransferase (cob(II)alamin reducing); aqCbl reductase; aquacobalamin reductase; cblE; methionine synthase reductase; methionine synthase reductase, mitochondrial; MSR
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9UBK8
  • Protein Name
    Methionine synthase reductase
  • Scientific Description
    This gene encodes a member of the ferredoxin-NADP(+) reductase (FNR) family of electron transferases. This protein functions in the synthesis of methionine by regenerating methionine synthase to a functional state. Because methionine synthesis requires methyl-group transfer by a folate donor, activity of the encoded enzyme is important for folate metabolism and cellular methylation. Mutations in this gene can cause homocystinuria-megaloblastic anemia, cbl E type. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2015]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203