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DNMT1 antibody (pSer714)
This Rabbit Polyclonal antibody specifically detects DNMT1 in IF. It exhibits reactivity toward Human.
Catalog No. ABIN7265030
$601.80
$708.00
save $106.20 (-15 %)
Plus shipping costs $50.00
60 μL ABIN7012611
120 μL ABIN7265029
200 μL ABIN7265030
60 μL ABIN7012611
120 μL ABIN7265029
200 μL ABIN7265030
Delivery in 11 to 14 Business Days
Quick Overview for DNMT1 antibody (pSer714) (ABIN7265030)
Target
See all DNMT1 Antibodies
DNMT1
(DNA (Cytosine-5)-Methyltransferase 1 (DNMT1))
Reactivity
All reactivities for DNMT1 antibodies
Human
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
pSer714
Characteristics
Phosphorylated antibody
Purification
Affinity purification
Immunogen
A synthetic phosphorylated peptide around S714 of human Dnmt1 (NP_001370.1).
Isotype
IgG
Alternatives
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Application Details
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Application Notes
IF 1:50-1:200
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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