WBSCR22 anticorps (C-Term)

N° du produit ABIN2789228

L’anticorps Lapin Polyclonal anti-WBSCR22 a été validé pour WB. Il convient pour détecter WBSCR22 dans des échantillons de Humain, Souris, Rat, Chien, Boeuf (Vache), Cobaye, Cheval, Porc et Lapin.

Aperçu rapide pour WBSCR22 anticorps (C-Term) (ABIN2789228)

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

Reactivité: Humain, Souris, Rat, Chien, Boeuf (Vache), Cobaye, Cheval, Porc, Lapin

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WBSCR22 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-WBSCR22 anticorps

Épitope: C-Term

Séquence: GGAFERRGIR GHQTRRFPLR MSRRGMVRKS RAWVLEKKER HRRQGREVRP

Homologie: Cow: 77%, Dog: 86%, Guinea Pig: 79%, Horse: 86%, Human: 100%, Mouse: 86%, Pig: 86%, Rabbit: 93%, Rat: 86%

Attributs du produit: This is a rabbit polyclonal antibody against WBSCR22. It was validated on Western Blot.

Purification: Affinity Purified

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 298 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

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. Alternatively spliced transcript variants have been found.
Alias Symbols: HASJ4442, HUSSY-3, MGC19709, MGC2022, MGC5140, PP3381, WBMT
Protein Interaction Partner: VCP, UBC, PKN1, OAS1, ZMYM3, THOC2, WDR74, REM1, PHLPP1, PPIP5K1, CUL3, SUMO2,
Protein Size: 298

Poids moléculaire: 32 kDa

ID gène: 114049

NCBI Accession: NM_001202560, NP_001189489

UniProt: C9K060