WBSCR16 产品
(Williams-Beuren Syndrome Chromosome Region 16 (WBSCR16))
Categories
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, Jul 2008].
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Featured WBSCR16 Categories
WBSCR16 抗体
High quality antibodies with extensive validation data.
WBSCR16 蛋白
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended WBSCR16 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB
Validations
- (1)
Cat. No.
ABIN529349
Quantity
50 μg
Datasheet
Datasheet
Reactivity
Human
Application
WB
Validations
- (1)
Cat. No.
ABIN6750694
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB
Validations
- (1)
Cat. No.
ABIN7271367
Quantity
100 μL
Datasheet
Datasheet
Recommended WBSCR16 ELISA试剂盒
Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Analytical Method
Quantitative Sandwich ELISA
Validations
Cat. No.
ABIN6234060
Quantity
96 tests
Datasheet
Datasheet
Recommended WBSCR16 蛋白
Synonyms and alternative names related to WBSCR16
RCC1 like (RCC1L), reculator of chromosome condensation 1 like (Rcc1l), 5730496C04Rik, AU019812Protein level used designations for WBSCR16
- RCC1-like G exchanging factor-like protein
- Williams-Beuren syndrome chromosomal region 16 protein
- Williams-Beuren syndrome chromosomal region 16 protein homolog
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