WBSCR22 Produkte
(Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
Kategorien
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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Ausgewählte WBSCR22 Kategorien
WBSCR22 Antikörper
High quality antibodies with extensive validation data.
WBSCR22 Proteine
Proteins for various applications incl. WB, ELISA, IF etc.
Empfohlene WBSCR22 Antikörper
Produkt
Reaktivität
Applikation
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität
Human, Mouse
Applikation
WB, IF, IP, IHC (p), ICC
Validierungen
- (1)
- (5)
Kat. Nr.
ABIN2856201
Menge
100 μL
Datenblatt
Datenblatt
Reaktivität
Human
Applikation
WB, IF, ELISA, IP
Validierungen
- (4)
Kat. Nr.
ABIN530242
Menge
100 μg
Datenblatt
Datenblatt
Reaktivität
Human, Rat
Applikation
IF, IHC
Validierungen
- (3)
Kat. Nr.
ABIN7263325
Menge
200 μL
Datenblatt
Datenblatt
Empfohlene WBSCR22 Proteine
Produkt
Reaktivität
Source
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität
Human
Source
Wheat germ
Validierungen
- (1)
Kat. Nr.
ABIN1325181
Menge
10 μg
Datenblatt
Datenblatt
Reaktivität
Human
Source
Wheat germ
Validierungen
- (1)
Kat. Nr.
ABIN1325180
Menge
25 μg
Datenblatt
Datenblatt
Reaktivität
Human
Source
Escherichia coli (E. coli)
Validierungen
- (1)
Kat. Nr.
ABIN2735489
Menge
50 μg
Datenblatt
Datenblatt
Neueste Publikationen zu unseren WBSCR22 Produkten
: "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).
Synonyme und alternative Namen zu 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:162306Bezeichner auf Proteinebene für 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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