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DNMT1
Anti-DNMT1 Recombinant Antibody Products
- PE-A2/Human DNMT1 (GLIEKNIEL) MHC Tetramer (MHC-LC1940)
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- Class: Class I
- Antigen: DNMT1
- Antigen Species: Human
- Peptide: GLIEKNIEL
- Conjugate: PE
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- APC-A2/Human DNMT1 (GLIEKNIEL) MHC Tetramer (MHC-LC1955)
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- Class: Class I
- Antigen: DNMT1
- Antigen Species: Human
- Peptide: GLIEKNIEL
- Conjugate: APC
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- Mouse Anti-DNMT1 Recombinant Antibody (clone CBS388) (MRO-A1926-YJ)
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- Species Reactivity: Human, Mouse, Zebrafish
- Type: Mouse IgG2b
- Application: WB, ELISA
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- PE-A*02:01/Human DNMT1 (GLIEKNIEL) MHC Tetramer (MHC-LC1982)
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- Class: Class I
- Antigen: DNMT1
- Antigen Species: Human
- Peptide: GLIEKNIEL
- Conjugate: PE
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- PE-A*01:01/Human DNMT1 (YLDDPDLKY) MHC Tetramer (MHC-LC2374)
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- Class: Class I
- Antigen: DNMT1
- Antigen Species: Human
- Peptide: YLDDPDLKY
- Conjugate: PE
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- APC-A*01:01/Human DNMT1 (YLDDPDLKY) MHC Tetramer (MHC-LC4421)
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- Class: Class I
- Antigen: DNMT1
- Antigen Species: Human
- Peptide: YLDDPDLKY
- Conjugate: APC
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- PE-A*02:01/Human DNMT1 (YLDDPDLKY) MHC Tetramer (MHC-LC4422)
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- Class: Class I
- Antigen: DNMT1
- Antigen Species: Human
- Peptide: YLDDPDLKY
- Conjugate: PE
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- PE-B*15:01/Human DNMT1 (YLDDPDLKY) MHC Tetramer (MHC-LC4423)
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- Class: Class I
- Antigen: DNMT1
- Antigen Species: Human
- Peptide: YLDDPDLKY
- Conjugate: PE
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- Rabbit Anti-DNMT1 Recombinant Antibody (clone JF09-89) (MRO-0486-CN)
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- Species Reactivity: Human, Mouse, Rat
- Type: Rabbit IgG
- Application: WB, IF, IHC
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- Chicken Anti-DNMT1 Polyclonal IgY (BRD-0164MZ)
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- Species Reactivity: Human
- Type: Chicken antibody
- Application: WB
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For Research Use Only. Not For Clinical Use.
This gene encodes an enzyme that transfers methyl groups to cytosine nucleotides of genomic DNA. This protein is the major enzyme responsible for maintaining methylation patterns following DNA replication and shows a preference for hemi-methylated DNA. Methylation of DNA is an important component of mammalian epigenetic gene regulation. Aberrant methylation patterns are found in human tumors and associated with developmental abnormalities. Variation in this gene has been associated with cerebellar ataxia, deafness, and narcolepsy, and neuropathy, hereditary sensory, type IE. Alternative splicing results in multiple transcript variants.