Anti-KMT2D / MLL2 antibody - N-terminal (ab199271)

Overview

  • Product name
    Anti-KMT2D / MLL2 antibody - N-terminal
    See all KMT2D / MLL2 primary antibodies
  • Description
    Rabbit polyclonal to KMT2D / MLL2 - N-terminal
  • Specificity
    ab199271 detects endogenous levels of total KMT2D protein.
  • Tested applications
    Suitable for: IHC-Pmore details
  • Species reactivity
    Reacts with: Human
  • Immunogen

    Synthetic peptide corresponding to Human KMT2D/ MLL2 (N terminal). NP_003473.3.
    Database link: O14686

  • Positive control
    • Human brain tissue.

Properties

Applications

Our Abpromise guarantee covers the use of ab199271 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
IHC-P 1/50 - 1/200.

Target

  • Function
    Histone methyltransferase. Methylates 'Lys-4' of histone H3 (H3K4me). H3K4me represents a specific tag for epigenetic transcriptional activation. Plays a central role in beta-globin locus transcription regulation by being recruited by NFE2. Acts as a coactivator for estrogen receptor by being recruited by ESR1, thereby activating transcription. Plays an important role in controlling bulk H3K4me during oocyte growth and preimplantation development. Required during the transcriptionally active period of oocyte growth for the establishment and/or maintenance of bulk H3K4 trimethylation (H3K4me3), global transcriptional silencing that preceeds resumption of meiosis, oocyte survival and normal zygotic genome activation.
  • Tissue specificity
    Expressed in most adult tissues, including a variety of hematoipoietic cells, with the exception of the liver.
  • Involvement in disease
    Defects in MLL2 are the cause of Kabuki syndrome (KABS) [MIM:147920]. It is a congenital mental retardation syndrome with additional features, including postnatal dwarfism, a peculiar facies characterized by long palpebral fissures with eversion of the lateral third of the lower eyelids, a broad and depressed nasal tip, large prominent earlobes, a cleft or high-arched palate, scoliosis, short fifth finger, persistence of fingerpads, radiographic abnormalities of the vertebrae, hands, and hip joints, and recurrent otitis media in infancy.
  • Sequence similarities
    Belongs to the histone-lysine methyltransferase family. TRX/MLL subfamily.
    Contains 1 FY-rich C-terminal domain.
    Contains 1 FY-rich N-terminal domain.
    Contains 5 PHD-type zinc fingers.
    Contains 1 post-SET domain.
    Contains 4 RING-type zinc fingers.
    Contains 1 SET domain.
  • Domain
    LXXLL motifs 5 and 6 are essential for the association with ESR1 nuclear receptor.
  • Post-translational
    modifications
    Phosphorylated upon DNA damage, probably by ATM or ATR.
  • Cellular localization
    Nucleus.
  • Information by UniProt
  • Database links
  • Alternative names
    • AAD10 antibody
    • ALL1 related gene antibody
    • ALL1-related protein antibody
    • ALR antibody
    • CAGL114 antibody
    • Histone-lysine N-methyltransferase MLL2 antibody
    • KABUK1 antibody
    • Kabuki make up syndrome antibody
    • Kabuki mental retardation syndrome antibody
    • KMS antibody
    • KMT2B antibody
    • KMT2D antibody
    • Lysine N methyltransferase 2D antibody
    • Lysine N-methyltransferase 2B antibody
    • MLL2 antibody
    • MLL2_HUMAN antibody
    • MLL4 antibody
    • Myeloid/lymphoid or mixed lineage leukemia 2 antibody
    • Myeloid/lymphoid or mixed-lineage leukemia protein 2 antibody
    • TNRC21 antibody
    • Trinucleotide repeat containing 21 antibody
    see all

Images

  • Immunohistochemical analysis of paraffin-embedded Human brain tissue labeling KMT2D / MLL2 with ab199271 at 1/40 dilution.

References

ab199271 has not yet been referenced specifically in any publications.

Customer reviews and Q&As

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Application
ChIP
Sample
Human Cell lysate - nuclear (K562 (human erythroid cell line))
Negative control
Normal IgG
Specification
K562 (human erythroid cell line)
Detection step
Taqman
Type
Cross-linking (X-ChIP)
Duration of cross-linking step: 10 minute(s) and 0 second(s)
Specification of the cross-linking agent: 1% formaldehyde
Positive control
NF-E2 antibody
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Submitted Oct 02 2015

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