WBSCR22 产品
(Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
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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. [provided by RefSeq, Feb 2011].
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Featured WBSCR22 Categories
WBSCR22 抗体
High quality antibodies with extensive validation data.
WBSCR22 蛋白
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended WBSCR22 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human, Mouse
Application
WB, IF, IP, IHC (p), ICC
Validations
- (1)
- (5)
Cat. No.
ABIN2856201
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB, IF, ELISA, IP
Validations
- (4)
Cat. No.
ABIN530242
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human, Rat
Application
IF, IHC
Validations
- (3)
Cat. No.
ABIN7263325
Quantity
200 μL
Datasheet
Datasheet
Recommended WBSCR22 蛋白
Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Source
Wheat germ
Validations
- (1)
Cat. No.
ABIN1325181
Quantity
10 μg
Datasheet
Datasheet
Reactivity
Human
Source
Wheat germ
Validations
- (1)
Cat. No.
ABIN1325180
Quantity
25 μg
Datasheet
Datasheet
Reactivity
Human
Source
Escherichia coli (E. coli)
Validations
- (1)
Cat. No.
ABIN2735489
Quantity
50 μg
Datasheet
Datasheet
Latest Publications for our WBSCR22 Products
: "Cardiac mitochondrial function depends on BUD23 mediated ribosome programming." in: eLife, Vol. 9, (2020) (PubMed).: "The human 18S rRNA base methyltransferases DIMT1L and WBSCR22-TRMT112 but not rRNA modification are required for ribosome biogenesis." in: Molecular biology of the cell, Vol. 26, Issue 11, pp. 2080-95, (2015) (PubMed).
: "The novel metastasis promoter Merm1/Wbscr22 enhances tumor cell survival in the vasculature by suppressing Zac1/p53-dependent apoptosis." in: Cancer research, Vol. 71, Issue 3, pp. 1146-55, (2011) (PubMed).
: "hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes." in: Genomics, Vol. 89, Issue 3, pp. 307-15, (2007) (PubMed).
: "Nucleolar proteome dynamics." in: Nature, Vol. 433, Issue 7021, pp. 77-83, (2005) (PubMed).
: "Identification of additional transcripts in the Williams-Beuren syndrome critical region." in: Human genetics, Vol. 110, Issue 5, pp. 429-38, (2002) (PubMed).
: "Characterization of 16 novel human genes showing high similarity to yeast sequences." in: Yeast (Chichester, England), Vol. 18, Issue 1, pp. 69-80, (2001) (PubMed).
Synonyms and alternative names related to WBSCR22
Williams-Beuren syndrome chromosome region 22 (WBSCR22), BUD23, rRNA methyltransferase and ribosome maturation factor L homeolog (bud23.L), BUD23, rRNA methyltransferase and ribosome maturation factor (bud23), williams Beuren syndrome chromosome region 22 (CpipJ_CPIJ001394), williams Beuren syndrome chromosome region 22 (PAAG_00857), williams Beuren syndrome chromosome region 22 (MCYG_07273), hypothetical protein (PGTG_07527), hypothetical protein (PGTG_12505), BUD23, rRNA methyltransferase and ribosome maturation factor (BUD23), BUD23, rRNA methyltransferase and ribosome maturation factor (Bud23), 1110003N24Rik, hasj4442, HASJ4442, hussy-3, HUSSY-3, MERM1, MGC82375, pp3381, PP3381, wbmt, WBMT, zgc:162306Protein level used designations for WBSCR22
- Williams Beuren syndrome chromosome region 22 protein
- Williams Beuren syndrome chromosome region 22
- hypothetical protein LOC496966
- williams Beuren syndrome chromosome region 22
- Williams-Beuren candidate region putative methyltransferase
- Williams-Beuren syndrome chromosomal region 22 protein
- metastasis-related methyltransferase 1
- uncharacterized methyltransferase WBSCR22
- Williams-Beuren syndrome chromosomal region 22 protein homolog
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