NIPBL Goat anti-Bovine, Dog, Human, Mouse, Orangutan, Rat, Polyclonal Antibody, Abnova™
Manufacturer: Abnova Corporation
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | 89-114-707-Each-of-1 | In Stock | ₹ 1,04,664.00 |
89-114-707 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 1,04,664.00
GST (18%): ₹ 18,839.52
Total Price: ₹ 1,23,503.52
Antigen
NIPBL
Classification
Polyclonal
Description
Goat polyclonal antibody raised against synthetic peptide of NIPBL.
Formulation
In 20mM KH2PO4, 150mM NaCl, pH 7.2 (0.01% sodium azide)
Gene Alias
CDLS/CDLS1/DKFZp434L1319/FLJ11203/FLJ12597/FLJ13354/FLJ13648/FLJ44854/IDN3/IDN3-B
Host Species
Goat
Quantity
100 μg
Primary or Secondary
Primary
Test Specificity
This affinity purified antibody is directed against human IDN3 protein.
Content And Storage
Store at 4°C. For long term storage store at -20°C.Aliquot to avoid repeated freezing and thawing.
Applications
ELISA, Western Blot
Conjugate
Unconjugated
Dilution
ELISA (1:2000-1:10000) Western Blot (1:500-1:3000) The optimal working dilution should be determined by the end user.
Gene
NIPBL
Gene Symbols
NIPBL
Immunogen
A synthetic peptide corresponding to amino acids 344-356 of human NIPBL.
Regulatory Status
RUO
Gene ID (Entrez)
25836
Target Species
Bovine, Canine, Human, Mouse, Orangutan, Rat
Form
Liquid
Related Products
Description
- This gene encodes the homolog of the Drosophila melanogaster Nipped-B gene product and fungal Scc2-type sister chromatid cohesion proteins
- The Drosophila protein facilitates enhancer-promoter communication of remote enhancers and plays a role in developmental regulation
- It is also homologous to a family of chromosomal adherins with broad roles in sister chromatid cohesion, chromosome condensation, and DNA repair
- The human protein has a bipartite nuclear targeting sequence and a putative HEAT repeat
- Condensins, cohesins and other complexes with chromosome-related functions also contain HEAT repeats
- Mutations in this gene result in Cornelia de Lange syndrome, a disorder characterized by dysmorphic facial features, growth delay, limb reduction defects, and mental retardation
- Two transcript variants encoding different isoforms have been found for this gene
- [provided by RefSeq