DNMT3B Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | 01-674-425-Each-of-1 | In Stock | ₹ 28,613.50 |
01-674-425 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 28,613.50
GST (18%): ₹ 5,150.43
Total Price: ₹ 33,763.93
Antigen
DNMT3B
Classification
Polyclonal
Conjugate
Unconjugated
Gene
Dnmt3b
Gene Alias
DNA (cytosine-5-)-methyltransferase 3 beta; DNA (cytosine-5)-methyltransferase 3B; DNA methyltransferase 3 beta; DNA methyltransferase 3B; DNA methyltransferase HsaIIIB; DNA methyltransferase MmuIIIB; DNA MTase HsaIIIB; DNA MTase MmuIIIB; Dnmt3; DNMT3B; ICF; ICF1; M.HsaIIIB; m.MmuIIIB; MGC1090; MmuIIIB
Host Species
Chicken
Purification Method
IgY fraction
Regulatory Status
RUO
Gene ID (Entrez)
1789
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Western Blot
Concentration
1 mg/mL
Formulation
PBS with 0.02% sodium azide
Gene Accession No.
Q9UBC3
Gene Symbols
Dnmt3b
Immunogen
Purified recombinant DNMT3L.1 corresponding to the chromosome 21 gene (Human).
Quantity
500 μg
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgY
Related Products
Description
- PA1-9542 detects DNMT3L in human samples
- PA1-9542 has been successfully used in Western blot procedures
- By Western blot, PA1-9542 detects a 47 kDa protein representing DNMT3L
- PA1-9542 immunogen is a purified recombinant DNMT3L.1 corresponding to the chromosome 21 gene (Human)
- CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation
- Studies in mice have demonstrated that DNA methylation is required for mammalian development
- This gene encodes a DNA methyltransferase which is thought to function in de novo methylation, rather than maintenance methylation
- The protein localizes primarily to the nucleus and its expression is developmentally regulated
- Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome
- Six alternatively spliced transcript variants have been described
- The full length sequences of variants 4 and 5 have not been determined.