Current Position:Home>>Antibodies>>Polyclonal Antibody>> HGH1 Polyclonal Antibody
Catalog number:E-AB-30673
Synonyms:Brain protein 16,BRP16,C8orf30A,chromosome 8 open reading frame 30A,D15Ertd741e,F203A,Fam203a,Family with sequence similarity 203 member A,FLJ40907,LOC51236,MGC94185,MNCb-5873,Protein FAM203A
Host: Rabbit
Reactivity: H,M,R
Applications: WB,IHC-p,ELISA
Lead Time: 7~10 daysWelcome to order from local distributors.
Add to cart Compare Bulk request ManualSynonyms | Brain protein 16,BRP16,C8orf30A,chromosome 8 open reading frame 30A,D15Ertd741e,F203A,Fam203a,Family with sequence similarity 203 member A,FLJ40907,LOC51236,MGC94185,MNCb-5873,Protein FAM203A |
Swissprot | Q9BTY7 |
Source | Rabbit |
Reactivity | Human,Mouse,Rat |
Immunogen | Synthesized peptide derived from the Internal region of human Brp16 |
Application | WB,IHC-p,ELISA |
Recommended dilution | WB 1:500-1:2000, IHC 1:100-1:300, ELISA 1:40000 |
Concentration | 1mg/mL |
Clonality | Polyclonal |
Isotype | IgG |
Purification | Affinity purification |
Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
Storage buffer | PBS with 0.02% sodium azide,0.5% BSA and 50% glycerol pH 7.4. |
Background | 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. |