WBSCR22 anticorps (AA 1-233)

N° du produit ABIN1885820

L’anticorps anti-WBSCR22 Polyclonal Lapin est utilisé pour la détection de WBSCR22 dans des échantillons de Humain. Il a été validé pour WB et IHC.

Aperçu rapide pour WBSCR22 anticorps (AA 1-233) (ABIN1885820)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WBSCR22 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Détail du produit anti-WBSCR22 anticorps

Épitope: AA 1-233

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 233 of Human WBSCR22

Information d'application

Indications d'application: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.100-1.250

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: Biohazard Informations: This product contains thimerosal which is hazardous.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Détails sur WBSCR22

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

Autre désignation: WBSCR22

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.[provided by RefSeq]

Poids moléculaire: 32 kDa

ID gène: 114049

NCBI Accession: NP_059998, NM_017528