Invitrogen™ FKSG2 Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA5103413

Catalog No. PIPA5103413

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.

Specifications

• 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