KMT2D Polyclonal Antibody | G-AB-02878

KMT2D Polyclonal Antibody | G-AB-02878 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas: Epigenetics and Nuclear Signaling

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

Reactivity: Human

Host: Rabbit

Isotype: IgG

Gene ID:

Accession #: NP_003473

Clonality: Polyclonal

Immunogen: Synthetic peptide of human KMT2D

Clone #:

Conjugation: Unconjugated

Swissprot: O14686

Santa Cruz: sc-68671/sc-68672/sc-292359

Calculated MW:

Observed MW:

Concentration: 0.4 mg/mL

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification method: Affinity purification

Application: IHC, ELISA

Dilution: IHC 1:50-1:200

Storage: Store at -20°C. Avoid freeze / thaw cycles.

KMT2D Polyclonal Antibody DataSheet