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Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody

Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody

Manufacturer	Abbexa
Category	Antibodies Cell Biology Immunohistochemistry Western Blot Immunofluorescence Immunocytochemistry Cell Stainings ECM Primary Antibodies
Type	Antibody Primary
Specific against	Human
Isotype	IgG
Applications	WB, IF, IHC, ICC
Amount	100 ul
Host	Rabbit
Item no.	abx005524-100
Targets	ELN
Conjugate/Tag	Unconjugated
eClass 6.1	32160702
eClass 9.0	32160702
Available
Antigen	WBSCR22
Description	WBSCR22 Antibody is a Rabbit Polyclonal antibody against WBSCR22. This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found.
Conjugation	Unconjugated
Purification	Affinity purified.
Storage	Aliquot and store at -20C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC	O43709
UniProt Entry Name	BUD23_HUMAN
Gene Symbol	BUD23
Gene ID	114049
Molecular Weight	Calculated MW: 24 kDa, 31 kDa, 33 kDa Observed MW: 36 kDa
Buffer	PBS, pH 7.3, 0.02% sodium azide, 50% glycerol.
Dry Ice	No
Note	This product is for research use only.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

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