PIPA5103413
FKSG2 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5103413-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA5103413 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
FKSG2
Classification
Polyclonal
Conjugate
Unconjugated
Gene
TPT1P8
Gene Alias
FKSG2; TPT1P8; tumor protein, translationally-controlled 1 pseudogene 8
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
59347
Content And Storage
-20°C
Form
Liquid
Applications
Immunohistochemistry (Paraffin), Western Blot
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Gene Accession No.
Q9HAU6
Gene Symbols
TPT1P8
Immunogen
A synthesized peptide derived from human TPT1P8(Accession Q9HAU6), corresponding to amino acid residues S81-T131.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Antibody detects endogenous levels of total FKSG2
- Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes
- Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis
- Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder
- Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects
- WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome
- Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome
- The FKSG2 gene product has been provisionally designated FKSG2 pending further characterization.