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DMGDH (DGR32797) Rabbit mAb
db13362
Datasheet
- 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. [provided by RefSeq, Jul 2013]
- Immunogen A synthetic peptide of human DMGDH
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Gene ID
29958
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Swiss Prot
Q9UI17
- Synonyms DMGDHD; ME2GLYDH
- Reactivity Human,Mouse,Rat
- Application WB
- Recommended dilution WB: 1:1000
- Calculated MW 97 kDa
- Observed MW 97 kDa
- Host species Rabbit
- Clonality Monoclonal
- Clonality No. DGR32797
- Isotype IgG
- Purity Affinity Purification
- Conjugation Un-conjugated
- Storage/Stability Store at -20°C. Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.
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Western blot analysis of extracts from Human fetal liver tissue using db13362 at 1:1000.
订购信息
- Package Price (RMB)
- 10μL 398
- 20μL 698
- 50μL 1398
- 100μL 2398
- 货期：现货
相关产品
For research use only. Not intended for diagnostic.
