C1orf57 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5117526-Each-of-1 | In Stock | ₹ 47,392.50 |
PIPA5117526 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 47,392.50
GST (18%): ₹ 8,530.65
Total Price: ₹ 55,923.15
Antigen
C1orf57
Classification
Polyclonal
Conjugate
Unconjugated
Gene
Ntpcr
Gene Alias
2310079N02Rik; AI449709; C1orf57; cancer-related nucleoside-triphosphatase; Cancer-related nucleoside-triphosphatase homolog; CH1073-266P11.1; HCR-NTPase; NTPase; Ntpcr; Nucleoside triphosphate phosphohydrolase; nucleoside-triphosphatase C1orf57 homolog; nucleoside-triphosphatase, cancer-related; RGD1306192; RP4-659I19.2; RP4-678E16.2; zgc:92420
Host Species
Rabbit
Purification Method
Protein G
Regulatory Status
RUO
Gene ID (Entrez)
445069
Content And Storage
-20°C or -80°C if preferred
Form
Liquid
Applications
Western Blot
Concentration
4.241 mg/mL
Formulation
10mM PBS with 50% glycerol and 0.03% ProClin 300; pH 7.4
Gene Accession No.
0
Gene Symbols
Ntpcr
Immunogen
Recombinant Zebrafish Nucleoside-triphosphatase, cancer-related protein (1-185aa)
Quantity
100 μg
Primary or Secondary
Primary
Target Species
Zebrafish
Product Type
Antibody
Isotype
IgG
Related Products
Description
- This antibody has been tested in direct-ELISA Belonging to the THEP1 NTPase family, C1orf57 (also known as nucleoside triphosphate phosphohydrolase), and its mouse homolog, 2310079N02Rik, are 190 amino acid proteins that has nucleotide phosphatase activity towards ATP, GTP, TTP, CTP and UTP
- Acting as a monomer, it also hydrolyzes nucleoside diphosphates with lower efficiency
- The gene encoding C1orf57 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome
- There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1
- Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A
- When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs
- The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration
- The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis
- Stickler syndrome, Parkinson's, Gaucher disease and Usher syndrome are also associated with chromosome 1.