SCYL1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA529295-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA529295 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
SCYL1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
Scyl1
Gene Alias
105 kDa kinase-like protein; 2810011O19Rik; C85140; Coated vesicle-associated kinase of 90 kDa; CVAK90; GKLP; HT019; likely ortholog of mouse N-terminal kinase-like protein; mdf; mfd; Mitosis-associated kinase-like protein NTKL; NKTL; N-terminal kinase-like protein; NTKL; P105; SCAR21; SCY1 like pseudokinase 1; SCY1-like 1 (S. cerevisiae); SCY1-like 1 splice variant 13; SCY1-like 1 splice variant 15; SCY1-like protein 1; SCY1-like, kinase-like 1; Scyl1; TAPK; TEIF; Telomerase regulation-associated protein; Telomerase transcriptional element-interacting factor; telomerase transcriptional elements-interacting factor; teratoma-associated tyrosine kinase; TRAP; ubiquitous protein kinase-like (105 kDa)
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
57410
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Immunocytochemistry, Western Blot
Concentration
1 mg/mL
Formulation
0.1M tris glycine with 10% glycerol and 0.01% thimerosal; pH 7
Gene Accession No.
Q96KG9
Gene Symbols
Scyl1
Immunogen
Recombinant fragment corresponding to a region within amino acids 328 and 552 of Human SCYL1
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Recommended positive controls: A431, H1299, HeLa
- Predicted reactivity: Mouse (96%), Rat (94%), Xenopus laevis (83%), Bovine (97%)
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome
- The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks
- Atm mutation leads to the disorder known as ataxia-telangiectasia
- The blood disorders Sickle cell anemia and β thalassemia are caused by HBB gene mutations
- Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene
- Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.