WBSCR27 产品
(Williams Beuren Syndrome Chromosome Region 27 (WBSCR27))
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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. [provided by RefSeq, Jul 2008].
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Featured WBSCR27 Categories
WBSCR27 抗体
High quality antibodies with extensive validation data.
WBSCR27 蛋白
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended WBSCR27 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB, IHC
Validations
- (4)
Cat. No.
ABIN7271366
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB, ELISA
Validations
- (2)
Cat. No.
ABIN2752638
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human, Mouse
Application
WB
Validations
- (1)
Cat. No.
ABIN7258970
Quantity
200 μL
Datasheet
Datasheet
Recommended WBSCR27 蛋白
Synonyms and alternative names related to WBSCR27
methyltransferase like 27 (METTL27)Protein level used designations for WBSCR27
- Williams-Beuren syndrome chromosomal region 27 protein
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