E-AB-19647
HGH1 Polyclonal Antibody
Size
£106.20
Was £118.00
- SKU:
- E-AB-19647
- Additional Names:
- BRP16,Brain protein 16,C8orf30A,D15Ertd741e,F203A,FLJ40907,Fam203a,Family with sequence similarity 203 member A,LOC51236,MGC94185,MNCb-5873,Protein FAM203A,chromosome 8 open reading frame 30A
- Application:
- IHC
- Concentration:
- 0.7 mg/ml
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Elabscience
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
- Immunogen:
- Synthetic peptide of human HGH1
- Uniprot:
- Q9BTY7
- Synonyms:
- brain protein 16;brain protein 16-like;BRP16;BRP16L;C8orf30A;C8orf30B;FAM203A;FAM203B;family with sequence similarity 203, member A;family with sequence similarity 203, member B;protein FAM203A;protein FAM203B;protein HGH1 homolog
- Extra Details:
- HGH1, is also known as BRP16, Brp16 is a 256 amino acid protein encoded by a gene on human chromosome 8. 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.
- Shipping Conditions:
- Blue Ice