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Invitrogen™ Human Dnmt3b ELISA Kit

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Quantity:
5 x 96 Tests
96 Tests
Description
Human Dnmt3b quantitates human Dnmt3b in serum, plasma, supernatant. The assay will exclusively recognize both natural and recombinant human Dnmt3b.
CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a DNA methyltransferase which is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes primarily to the nucleus and its expression is developmentally regulated. Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome. Six alternatively spliced transcript variants have been described. The full length sequences of variants 4 and 5 have not been determined.

Specifications
Specifications
Accession Number | DNA (cytosine-5-)-methyltransferase 3 beta; DNA (cytosine-5)-methyltransferase 3 B; DNA methyltransferase 3 beta; DNA methyltransferase 3 B; DNA methyltransferase HsaIIIB; DNA methyltransferase MmuIIIB; DNA MTase HsaIIIB; DNA MTase MmuIIIB; Dnmt3; DNMT3B; ICF; ICF1; M.HsaIIIB; m.MmuIIIB; MGC1090; MmuIIIB |
Assay Range | 0.64 to 150 ng/mL |
Assay Sensitivity | 0.64 ng/mL |
Conjugate | HRP |
Product Type | ELISA |
Sample Type | Plasma, Serum, Supernatant |
For Use With (Equipment) | Colorimetric Microplate Reader |
Gene ID (Entrez) | 1789 |
Gene Symbol | Dnmt3b |
Interassay CV | <12% |
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Safety and Handling
WARNING: Reproductive Harm - www.P65Warnings.ca.gov
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