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Rabbit anti-Human BHMT Monoclonal Antibody

The antibody against BHMT was raised in Rabbit using the recombinant protein of human BHMT as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.

ADA-15297A

The antibody against BHMT was raised in Rabbit using the recombinant protein of human BHMT as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.

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Specifications


Cat.No ADA-15297A ClonalityMonoclonal
Host SpeciesRabbitTarget NameBHMT
Target SynonymsBHMT1; HEL-S-61p; BHMTFormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, 0.05% BSA, PBS with 0.05% proclin300, pH7.3.Purification MethodAffinity purification
Positive SamplesHep G2, Rat liverApplicationELISA, WB, IHC-P

Immunogen Information


Immunogen DescriptionRecombinant protein of human BHMT.Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ93088
Background Information
  • Uniprot Id

    Q93088

  • Target Species

    Human

  • Target Name

    BHMT

  • Target Full Name

    Betaine--homocysteine S-methyltransferase 1

  • Target Function

    Involved in the regulation of homocysteine metabolism. Converts betaine and homocysteine to dimethylglycine and methionine, respectively. This reaction is also required for the irreversible oxidation of choline.

  • Target Subcellular Location

    Cytoplasm.

  • Target Tissue Specificity

    Found exclusively in liver and kidney.

  • Target Synonyms

    Betaine homocysteine methyltransferase; Betaine homocysteine S methyltransferase 1; Betaine homocysteine S methyltransferase; Betaine--homocysteine S-methyltransferase 1; BHMT; BHMT1; BHMT1_HUMAN; EC 2.1.1.5; Epididymis secretory sperm binding protein Li 61p; HEL S 61p

  • Target Background

    This gene encodes a cytosolic enzyme that catalyzes the conversion of betaine and homocysteine to dimethylglycine and methionine, respectively. Defects in this gene could lead to hyperhomocyst(e)inemia, but such a defect has not yet been observed.

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