KMT2D Polyclonal Antibody (E-AB-15954)

For research use only.
Verified Samples |
Verified Samples in IHC: Human brain |
Dilution | IHC 1:50-1:200 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human |
Applications | IHC |
Clonality | Polyclonal |
Immunogen | Synthetic peptide of human KMT2D |
Abbre | KMT2D |
Synonyms | AAD10, ALL1 related gene, ALL1-related protein, ALR, CAGL114, Histone-lysine N-methyltransferase MLL2, KABUK1, KMS, KMT2B, KMT2D, Kabuki make up syndrome, Kabuki mental retardation syndrome, Lysine N methyltransferase 2D, Lysine N-methyltransferase 2B, M, MLL2, MLL4 |
Swissprot | |
Cellular Localization | Nucleus. |
Concentration | 0.4 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | Affinity purification |
Research Areas | Epigenetics and Nuclear Signaling |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
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. |
Other Clones
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Other Formats
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Unconjugated
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