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Invitrogen™ FKSG2 Polyclonal Antibody
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Catalog No. PIPA5103413
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PIPA5103413 100 μL
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Catalog No. PIPA5103413 Supplier Invitrogen™ Supplier No. PA5103413
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Rabbit Polyclonal Antibody

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.
TRUSTED_SUSTAINABILITY

Specifications

Antigen FKSG2
Applications Immunohistochemistry (Paraffin), Western Blot
Classification Polyclonal
Concentration 1 mg/mL
Conjugate Unconjugated
Formulation PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Gene TPT1P8
Gene Accession No. Q9HAU6
Gene Alias FKSG2; TPT1P8; tumor protein, translationally-controlled 1 pseudogene 8
Gene Symbols TPT1P8
Host Species Rabbit
Immunogen A synthesized peptide derived from human TPT1P8(Accession Q9HAU6), corresponding to amino acid residues S81-T131.
Purification Method Affinity Chromatography
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 59347
Target Species Human, Mouse
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG
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