WBS16 Antibody
Product Specifications
Background
This gene encodes an RCC1-like G-exchanging factor. It is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq].
NCBI Gene ID
81554
Swiss Prot
Q96I51
Accession Number
Q96I51
Host
Rabbit
Reactivity
Human, Hamster
Immunogen
This WBS16 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 15-44 amino acids from the N-terminal region of human WBS16.
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cell Cycle
Purification
This antibody is purified through a protein A column, followed by peptide affinity purification.
Concentration
Batch dependent
Buffer
Supplied in PBS with 0.09% (W/V) sodium azide.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at 4˚ C for three months and -20˚ C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Product Datasheet
https://www.prosci-inc.com/?datasheet_sku=57-380
Calculated Molecular Weight
50 kDa
Fragment
Rabbit Ig
Applications Notes
For WB starting dilution is: 1:1000
Symbol
WBSCR16
NCBI Official Name
Williams-Beuren syndrome chromosomal region 16 protein
NCBI Organism
Homo sapiens
Background Reference 01
Merla, G., et al. Hum. Genet. 110 (5) :429-438 (2002)
Other Product Names
Williams-Beuren syndrome chromosomal region 16 protein, RCC1-like G exchanging factor-like protein, WBSCR16
Tested Applications
WB
Protein ID
116242843
Physical Properties
Liquid
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