PIPA5143204
Nucleostemin Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5143204-Each-of-1 | In Stock | ₹ 40,317.00 |
PIPA5143204 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 40,317.00
GST (18%): ₹ 7,257.06
Total Price: ₹ 47,574.06
Antigen
Nucleostemin
Classification
Polyclonal
Conjugate
Unconjugated
Gene
GNL3
Gene Alias
C77032; E2IG3; E2-induced gene 3 protein; estradiol-induced nucleotide binding protein; G protein nucleolar 3; Gnl3; guanine nucleotide binding protein-like 3 (nucleolar); guanine nucleotide-binding protein-like 3; MGC800; NNP47; novel nucleolar protein 47; Ns; nucleolar GTP-binding protein 3; Nucleostemin
Host Species
Goat
Purification Method
Ammonium sulfate precipitation
Regulatory Status
RUO
Gene ID (Entrez)
26354
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles
Isotype
IgG
Applications
Western Blot
Concentration
0.5 mg/mL
Formulation
TBS with 0.5% BSA and 0.02% sodium azide; pH 7.3
Gene Accession No.
Q9BVP2
Gene Symbols
GNL3
Immunogen
Peptide with sequence C-EKNNAQSIRAIKGPH.
Quantity
100 μg
Primary or Secondary
Primary
Target Species
Human
Form
Liquid
Related Products
Description
- Additional Information: This antibody is expected to recognize both reported isoforms (NP_055181.3; NP_996561.1)
- This antibody is tested in Peptide ELISA: antibody detection limit dilution 1:128,000
- Arylsulfatase F, also known as ARSF, is a 590 amino acid secretory protein that belongs to the sulfatase family of bone and cartilage matrix proteins
- Arylsulfatase F uses calcium as a cofactor to catalyze reactions that are important in maintaining correct bone composition
- The activity of Arylsulfatase F, unlike that of other family members, such as Arylsulfatase E, is not inhibited by warfarin
- The gene encoding Arylsulfatase F maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes
- In conjunction with chromosome Y, chromosome X is responsible for sex determination
- There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.