Anti-Human KMT2D Polyclonal Antibody

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.
List Price: $398
  • Buy 5 for $378.1 each and save 5%
  • Buy 21 for $358.2 each and save 10%
  • Buy 31 for $338.3 each and save 15%
  • Buy 51 for

Properties

Data Sheet Click for Datasheet
Catalog Number PA10483
Size 100μl
Host Type Rabbit
Immunogen Synthetic peptide of human KMT2D
Specificity Expressed in most adult tissues, including a variety of hematoipoietic cells, with the exception of the liver.
Isotype IgG
Reacitivity Human
Clone
Uniprot O14686
Concentration 0.4 mg/mL
Dilution IHC 1:50-1:200
Formulation
Application IHC,ELISA
Other Names 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
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

© Copyright 2024 TZYBIOTECH. All Rights Reserved. SiteMap