WBSCR16 Antibody
Product Specifications
Background
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.
NCBI Gene ID
81554
Swiss Prot
Q96I51
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-230 of human WBSCR16 (NP_110425.2) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cell Cycle
Purification
Affinity purification
Positive Control
Raji
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: 50kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:2000
Symbol
WBSCR16
Positive Control 2
HeLa
Positive Control 3
LO2
Positive Control 4
Mouse liver
Positive Control 5
Rat liver
NCBI Official Name
Williams-Beuren syndrome chromosomal region 16 protein
NCBI Organism
Homo sapiens
Other Product Names
Williams-Beuren syndrome chromosomal region 16 protein, RCC1-like G exchanging factor-like protein, WBSCR16
Tested Applications
WB
Physical Properties
Liquid
Curated Selection
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