Anti-MTR Monoclonal Antibody (C-1D1)

Anti-MTR Monoclonal Antibody (C-1D1)

Cat No: ASZ1C1259

Summary
Host Species:
Mouse
Species Reactivity:
Human
Applications:
Immunohistochemistry, Immunocytochemistry, Western Blot, Immunoprecipitation
Clone ID:
C-1D1
Clonality:
Monoclonal

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Product Information
Subcat Description Isotype Antibody Modification Conjugate Size Price Quantity
ASZ1C1259 Anti-MTR Antibody (C-1D1) Mouse IgG None $460
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  • Anti-MTR Monoclonal Antibody (C-1D1)
    • Product Description:
      The Anti-MTR antibody is a mouse monoclonal antibody recommended for immunohistochemistry, immunocytochemistry, western blot, immunoprecipitation and other applications. This antibody specifically targets human MTR.
      Applications:
      Immunohistochemistry, Immunocytochemistry, Western Blot, Immunoprecipitation
      Source:
      Mouse
      Target:
      MTR
      Target Species:
      Human
      Specificity:
      This antibody reacts with human 5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR).
      Clonality:
      Monoclonal
      Clone ID:
      C-1D1
      Purification:
      The antibody was purified by affinity chromatography.
      Purity:
      >95% as determined by SDS-PAGE
      Concentration:
      1 mg/mL
      Form:
      Liquid
      Formulation:
      Contact us for custom product formulation.
      Preservative:
      0.02% sodium azide
      Shipping:
      Shipped at 4°C.
      Storage:
      This antibody can be stored at 2°C-8°C for one month. For longer storage, store at -20°C. Avoid repeated freeze-thaw cycles.
  • Anti-MTR Monoclonal Antibody (C-1D1) Applications
    • Recommended Dilution:
      Western Blot: 1:500-1:5000
      Immunohistochemistry: 1:50-1:200
      Immunocytochemistry: 1:50-1:200
      Note:
      Optimal dilutions/concentrations should be determined by the end user.
Protein Name
Methionine synthase
Introduction
This gene encodes the 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
Alternative Names
HMAG; MS; cblG
Gene ID
UniProt
Related Disease
Homocystinuria-megaloblastic anemia, cblG type (HMAG)
Subcellular Location
Cytoplasm
Cell Line Specificity
Low cancer specificity
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