WBSCR27 anticorps (N-Term)

N° du produit ABIN955542

Cet anticorps anti-WBSCR27 Polyclonal Lapin (ABIN955542) détecte spécifiquement WBSCR27 dans WB, IHC (p) et EIA. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour WBSCR27 anticorps (N-Term) (ABIN955542)

Antigène: WBSCR27 (Williams Beuren Syndrome Chromosome Region 27 (WBSCR27))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WBSCR27 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Détail du produit anti-WBSCR27 anticorps

Épitope: AA 12-42, N-Term

Specificité: This antibody detects WBSCR27 (N-term).

Réactivité croisée (Details): Species reactivity (tested):Human

Purification: Protein A column followed by peptide affinity purification

Immunogène: KLH conjugated synthetic peptide between 12-42 amino acids from the N-terminal region of human WBSCR27

Isotype: Ig Fraction

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS with 0.09 % (W/V) sodium azide

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 freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at 2 - 8 °C for up to six months or (in aliquots) at -20 °C for longer.

Détails sur WBSCR27

Antigène: WBSCR27 (Williams Beuren Syndrome Chromosome Region 27 (WBSCR27))

Autre désignation: WBSCR27

Sujet: WBSCR27 encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23Synonyms: Williams-Beuren syndrome chromosomal region 27 protein

ID gène: 155368

NCBI Accession: NP_689772