DMGDH polyclonal antibody

Catalog # PAB23001

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Price

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Quantity

Size:100 uL
Price: USD $ 428.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Application

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

Immunohistochemical staining of human kidney with DMGDH polyclonal antibody (Cat # PAB23001) shows strong granular cytoplasmic positivity in cells in tubules at 1:20-1:50 dilution.

  • Specification

    Product Description

    Rabbit polyclonal antibody raised against recombinant DMGDH.

    Immunogen

    Recombinant protein corresponding to amino acids of human DMGDH.

    Sequence

    TLATDDVDPEGNESIWYNGKVVGNTTSGSYSYSIQKSLAFAYVPVQLSEVGQQVEVELLGKNYPAVIIQEPLVLTEPTRNRLQK

    Host

    Rabbit

    Reactivity

    Human

    Form

    Liquid

    Purification

    Antigen affinity purification

    Isotype

    IgG

    Recommend Usage

    Immunohistochemistry (1:20-1:50)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, pH 7.2 (40% glycerol, 0.02% sodium azide)

    Storage Instruction

    Store at 4°C. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Immunohistochemical staining of human kidney with DMGDH polyclonal antibody (Cat # PAB23001) shows strong granular cytoplasmic positivity in cells in tubules at 1:20-1:50 dilution.
  • Gene Info — DMGDH

    Entrez GeneID

    29958

    Protein Accession#

    Q9UI17

    Gene Name

    DMGDH

    Gene Alias

    DMGDHD, ME2GLYDH

    Gene Description

    dimethylglycine dehydrogenase

    Omim ID

    605849 605850

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme is found as a monomer in the mitochondrial matrix, and uses flavin adenine dinucleotide and folate as cofactors. Mutation in this gene causes dimethylglycine dehydrogenase deficiency, characterized by a fishlike body odor, chronic muscle fatigue, and elevated levels of the muscle form of creatine kinase in serum. [provided by RefSeq

    Other Designations

    -

  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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