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Invitrogen™ KMT2D Polyclonal Antibody

Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA5115579
This item is not returnable.
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Description
Antibody detects endogenous levels of total MLL2.
KMT2D is a histone methyltransferase that methylates Lys-4 of histone H3 (H3K4me). H3K4me represents a specific tag for epigenetic transcriptional activation. KMT2D acts as a coactivator for estrogen receptors by being recruited by ESR1 and activating transcription. KMT2D is involved in chromatin organization, chormatin silencig, oocyte growth, oogenesis, and a positive regulation of cell proliferation. Mutations in the KMT2D gene cause Kabuki syndrome (KABUK1) which results in congential mental retardation syndrome.
Specifications
| KMT2D | |
| Polyclonal | |
| Unconjugated | |
| KMT2D | |
| AAD10; ALL1-related protein; ALR; CAGL114; Histone-lysine N-methyltransferase 2D; histone-lysine N-methyltransferase MLL2; KABUK1; Kabuki make-up syndrome; Kabuki mental retardation syndrome; KMS; KMT2D; lysine (K)-specific methyltransferase 2D; lysine methyltransferase 2D; lysine N-methyltransferase 2D; MLL2; MLL4; myeloid/lymphoid or mixed-lineage leukemia 2; Myeloid/lymphoid or mixed-lineage leukemia protein 2; TNRC21; trinucleotide repeat containing 21 | |
| Rabbit | |
| Affinity chromatography | |
| RUO | |
| 8085 | |
| -20°C | |
| Liquid |
| Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry | |
| 1 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide | |
| O14686 | |
| KMT2D | |
| A synthesized peptide derived from human KMT2D(Accession O14686), corresponding to amino acid residues G1967-T2017. | |
| 100 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
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