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DNMT1 antibody (acLys1127, acLys1129, acLys1131, acLys1133)
The Rabbit Polyclonal anti-DNMT1 antibody (ABIN7261536) specifically detects DNMT1 in IF.
The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7261536
$601.80
$708.00
save $106.20 (-15 %)
Plus shipping costs $50.00
60 μL ABIN7010717
120 μL ABIN7261535
200 μL ABIN7261536
60 μL ABIN7010717
120 μL ABIN7261535
200 μL ABIN7261536
Delivery in 11 to 14 Business Days
Quick Overview for DNMT1 antibody (acLys1127, acLys1129, acLys1131, acLys1133) (ABIN7261536)
Target
See all DNMT1 Antibodies
DNMT1
(DNA (Cytosine-5)-Methyltransferase 1 (DNMT1))
Reactivity
All reactivities for DNMT1 antibodies
Human, Mouse, Rat
Host
All hosts for DNMT1 antibodies
Rabbit
Clonality
All clonalities for DNMT1 antibodies
Polyclonal
Conjugate
All conjugates for DNMT1 antibodies
This DNMT1 antibody is un-conjugated
Application
All applications for DNMT1 antibodies
Immunofluorescence (IF)
Product Details anti-DNMT1 Antibody
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Binding Specificity
All epitopes for DNMT1 antibodies
acLys1127, acLys1129, acLys1131, acLys1133
Characteristics
Acetylated antibody
Purification
Affinity purification
Immunogen
A synthetic peptide of human DNMT1
Isotype
IgG
Alternatives
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Application Details
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Application Notes
IF 1:50-1:100
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
1 mg/mL
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 Details for DNMT1
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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.
Gene ID
1786
UniProt
P26358
Pathways
SARS-CoV-2 Protein Interactome , The Global Phosphorylation Landscape of SARS-CoV-2 Infection
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