FKSG2 polyclonal, anti-human, mouse, rat
€305.00
In stock
SKU
BS60077
Background:
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.
Alternative Name:
Putative translationally-controlled tumor protein-like protein TPT1P8, Putative apoptosis inhibitor FKSG2, TPT1P8, FKSG2
Application Dilution: WB: 1:500~1:1000
Specificity: FKSG2 polyclonal antibody detects endogenous levels of FKSG2 protein.
Immunogen:
A synthetic peptide corresponding to residues in Human FKSG2.
MW: ~ 15 kDa
Swis Prot.: Q9HAU6
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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.
Alternative Name:
Putative translationally-controlled tumor protein-like protein TPT1P8, Putative apoptosis inhibitor FKSG2, TPT1P8, FKSG2
Application Dilution: WB: 1:500~1:1000
Specificity: FKSG2 polyclonal antibody detects endogenous levels of FKSG2 protein.
Immunogen:
A synthetic peptide corresponding to residues in Human FKSG2.
MW: ~ 15 kDa
Swis Prot.: Q9HAU6
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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