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DMGDH Polyclonal Antibody

CAT: 0866-RD217889A-01Size: 20 µLDry Ice: NoHazardous: No
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CAT#:0866-RD217889A-01Size:20 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Background
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. Alternative splicing results in multiple transcript variants.
Description
This is a DMGDH Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.
Synonyms
Dimethylglycine dehydrogenase, Dimethylglycine dehydrogenase, mitochondrial, Dmgdh, M2GD, ME2GLYDH, mitochondrial
Swiss Prot
Q9UI17
Accession Number
NP037523
Reactivity
Human
Immunogen
Synthetic peptide of human DMGDH
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Polyclonal Antibody
Applications
WB, ELISA
Purification Method
Antigen affinity purification
Assay Type
Antibody
Concentration
2.1 mg/mL
Dilution
WB 1:500-1:2000, ELISA 1:5000-1:10000
Buffer
PBS with 0.05% NaN3 and 40% Glycerol, pH7.4
Storage Conditions
Store at -20°C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
97 kDa
Observed Molecular Weight
Refer to figures
Host or Source
Rabbit
Isotype
IgG

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