Description
KMT2D Polyclonal Antibody | E-AB-15954 | Gentaur UK, US & Europe Distribution
Type: Polyclonal Antibody
Synonyms: AAD10, ALL1 related gene, ALL1-related protein, ALR, CAGL114, Histone-lysine N-methyltransferase MLL2, KABUK1, Kabuki make up syndrome, Kabuki mental retardation syndrome, KMS, KMT2B, KMT2D, Lysine N methyltransferase 2D, Lysine N-methyltransferase 2B, MLL2, MLL2, MLL4, Myeloid/lymphoid or mixed lineage leukemia 2, Myeloid/lymphoid or mixed-lineage leukemia protein 2, TNRC21, Trinucleotide repeat containing 21
Application: IHC, ELISA
Reactivity: Human
Host: Rabbit
Isotype: IgG
Reserch Areas: Epigenetics and Nuclear Signaling
Background: The protein encoded by this gene is a histone methyltransferase that methylates the Lys-4 position of histone H3. The encoded protein is part of a large protein complex called ASCOM, which has been shown to be a transcriptional regulator of the beta-globin and estrogen receptor genes. Mutations in this gene have been shown to be a cause of Kabuki syndrome.
Concentration: 0.4 mg/mL
Storage: Store at -20°C. Avoid freeze / thaw cycles.
Immunogen: Synthetic peptide of human KMT2D
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification Method: Affinity purification
Dilution: IHC 1:50-1:200
Clone: N/A
Conjugation: Unconjugated
Molecular Weight(Calculated): N/A
Molecular Weight(Observed): N/A