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DNMT1 antibody (acLys1127, acLys1129, acLys1131, acLys1133)

This Rabbit Polyclonal antibody specifically detects DNMT1 in IHC and IF. It exhibits reactivity toward Human.
Catalog No. ABIN6135487

Quick Overview for DNMT1 antibody (acLys1127, acLys1129, acLys1131, acLys1133) (ABIN6135487)

Target

See all DNMT1 Antibodies
DNMT1 (DNA (Cytosine-5)-Methyltransferase 1 (DNMT1))

Reactivity

  • 186
  • 41
  • 30
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

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  • 47
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Rabbit

Clonality

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  • 61
Polyclonal

Conjugate

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  • 1
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  • 1
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This DNMT1 antibody is un-conjugated

Application

  • 118
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Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

    • 22
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    • 1
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    • 1
    acLys1127, acLys1129, acLys1131, acLys1133

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Acetylated Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthetic peptide of human Acetyl-DNMT1-K1127/K1129/K1131/K1133

    Isotype

    IgG
  • Application Notes

    IHC,1:50 - 1:100,IF,1:50 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    DNMT1 (DNA (Cytosine-5)-Methyltransferase 1 (DNMT1))

    Alternative Name

    DNMT1

    Background

    This gene encodes an enzyme that transfers methyl groups to cytosine nucleotides of genomic DNA. This protein is the major enzyme responsible for maintaining methylation patterns following DNA replication and shows a preference for hemi-methylated DNA. Methylation of DNA is an important component of mammalian epigenetic gene regulation. Aberrant methylation patterns are found in human tumors and associated with developmental abnormalities. Variation in this gene has been associated with cerebellar ataxia, deafness, and narcolepsy, and neuropathy, hereditary sensory, type IE. Alternative splicing results in multiple transcript variants.,ADCADN,AIM,CXXC9,DNMT,HSN1E,MCMT,m.HsaI,DNMT1,Epigenetics & Nuclear Signaling,Chromatin Modifying Enzymes,DNA methylation,DNMT1

    Molecular Weight

    144 kDa/183 kDa/184 kDa

    Gene ID

    1786

    UniProt

    P26358

    Pathways

    SARS-CoV-2 Protein Interactome, The Global Phosphorylation Landscape of SARS-CoV-2 Infection
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