WBSCR27 Rabbit pAb
Sizes: 20μL, 100μL
Catalogue Numbers: A16176-20, A16176-100
Citations, Manuals and MSDS Available upon request.
Background: This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23.
Category: Polyclonal Antibodies
Applications: WB, IHC-P, ELISA
Cross-reactivity: Human, Mouse, Rat
Protein Weight: 27kDa
Observed Molecular Weight: 26kDa
Immunogen: Recombinant protein (or fragment)
Species: Human
GeneID: 155368
SWISS: Q8N6F8
Alternate Names: WBSCR27
Source: Rabbit
Isotype: IgG
Purity: Affinity purification
Storage: Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.01% thimerosal, 50% glycerol, pH 7.3.
Recommended Dilutions: WB, 1:500 - 1:2000 IHC-P, 1:50 - 1:200 ELISA, Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Research Areas: Cell Biology & Developmental Biology.
NCBI Alias: METTL27
Research Use Only