WBSCR22 Produits
(Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
Catégories
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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Catégories WBSCR22 en vedette
WBSCR22 Anticorps
High quality antibodies with extensive validation data.
WBSCR22 Protéines
Proteins for various applications incl. WB, ELISA, IF etc.
WBSCR22 recommandé Anticorps
Produit
Reactivity
Application
Validations
N° du produit
Quantité
Fiche technique
Reactivity
Human, Mouse
Application
WB, IF, IP, IHC (p), ICC
Validations
- (1)
- (5)
N° du produit
ABIN2856201
Quantité
100 μL
Fiche technique
Fiche technique
Reactivity
Human
Application
WB, IF, ELISA, IP
Validations
- (4)
N° du produit
ABIN530242
Quantité
100 μg
Fiche technique
Fiche technique
Reactivity
Human, Rat
Application
IF, IHC
Validations
- (3)
N° du produit
ABIN7263325
Quantité
200 μL
Fiche technique
Fiche technique
WBSCR22 recommandé Protéines
Produit
Reactivity
Source
Validations
N° du produit
Quantité
Fiche technique
Reactivity
Human
Source
Wheat germ
Validations
- (1)
N° du produit
ABIN1325181
Quantité
10 μg
Fiche technique
Fiche technique
Reactivity
Human
Source
Wheat germ
Validations
- (1)
N° du produit
ABIN1325180
Quantité
25 μg
Fiche technique
Fiche technique
Reactivity
Human
Source
Escherichia coli (E. coli)
Validations
- (1)
N° du produit
ABIN2735489
Quantité
50 μg
Fiche technique
Fiche technique
Dernières publications sur nos produits WBSCR22
: "Cardiac mitochondrial function depends on BUD23 mediated ribosome programming." dans: eLife, Vol. 9, (2020) (PubMed).: "The human 18S rRNA base methyltransferases DIMT1L and WBSCR22-TRMT112 but not rRNA modification are required for ribosome biogenesis." dans: 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." dans: 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." dans: Genomics, Vol. 89, Issue 3, pp. 307-15, (2007) (PubMed).
: "Nucleolar proteome dynamics." dans: Nature, Vol. 433, Issue 7021, pp. 77-83, (2005) (PubMed).
: "Identification of additional transcripts in the Williams-Beuren syndrome critical region." dans: Human genetics, Vol. 110, Issue 5, pp. 429-38, (2002) (PubMed).
: "Characterization of 16 novel human genes showing high similarity to yeast sequences." dans: Yeast (Chichester, England), Vol. 18, Issue 1, pp. 69-80, (2001) (PubMed).
Synonymes et noms alternatifs relatifs à 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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