WBSCR22 anticorps

N° du produit ABIN7263325

Détail du produit anti-WBSCR22 anticorps

Antigène: WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WBSCR22 est non-conjugé

Application: Immunofluorescence (IF), Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human WBSCR22 (NP_059998.2).

Isotype: IgG

Information d'application

Indications d'application: IHC 1:50-1:200 IF 1:50-1:100

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur WBSCR22

Antigène: WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

Autre désignation: WBSCR22 (WBSCR22 Produits)

Synonymes: anticorps MGC82375, anticorps wbmt, anticorps pp3381, anticorps hussy-3, anticorps hasj4442, anticorps zgc:162306, anticorps HASJ4442, anticorps HUSSY-3, anticorps MERM1, anticorps PP3381, anticorps WBMT, anticorps 1110003N24Rik, anticorps Williams-Beuren syndrome chromosome region 22, anticorps BUD23, rRNA methyltransferase and ribosome maturation factor L homeolog, anticorps BUD23, rRNA methyltransferase and ribosome maturation factor, anticorps williams Beuren syndrome chromosome region 22, anticorps hypothetical protein, anticorps WBSCR22, anticorps bud23.L, anticorps bud23, anticorps CpipJ_CPIJ001394, anticorps PAAG_00857, anticorps MCYG_07273, anticorps PGTG_07527, anticorps PGTG_12505, anticorps BUD23, anticorps Bud23

Sujet: 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.

ID gène: 114049

UniProt: O43709