WBSCR27 Antibody
Product Specifications
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.
NCBI Gene ID
155368
Swiss Prot
Q8N6F8
Host
Rabbit
Reactivity
Human, Mouse
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-245 of human WBSCR27 (NP_689772.2) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cell Cycle
Purification
Affinity purification
Positive Control
HT-29
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
Observed: 26kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:2000
Symbol
WBSCR27
Positive Control 2
MCF7
Positive Control 3
Mouse lung
NCBI Official Name
Methyltransferase like 27
NCBI Organism
Homo sapiens
Other Product Names
WBSCR27, methyltransferase-like protein 27, Williams Beuren syndrome chromosome region 27, williams-Beuren syndrome chromosomal region 27 protein
Tested Applications
WB
Physical Properties
Liquid
Curated Selection
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