RCC1L Polyclonal AntibodyE-AB-11679
Product Type: Antibody
Descritpion: This gene encodes a protein containing regulator of chromosome condensation 1-like repeats. The encoded protein may function as a guanine nucleotide exchange factor. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. Alternative splicing results in multiple transcript variants. RCC1L (RCC1 Like) is a Protein Coding gene. Diseases associated with RCC1L include Williams-Beuren Syndrome. An important paralog of this gene is RPGR.
Research Areas: Cell Biology
Recommended Dilutions: WB 1:200-1:1000, IHC 1:50-100
Size: 200 uL
Gene Accession: NP_110425
Immunogen: Synthetic peptide of human WBSCR16
Formulation: PBS with 0.05% sodium azide, 50% glycerol, PH7.3
Purification: Affinity purification
Calculated MW: 50kDa
Tissue Specificity/Positive Control: Ubiquitous.
Cellular Localization: Mitochondrion
Storage: Store at -20C. Avoid freeze / thaw cycles.
Product Link: https://www.elabscience.com/p-rcc1l_polyclonal_antibody-39698.html
Manual Link: https://www.elabscience.com/viewpdf-39698-elabscience-E-AB-11679.PDF