ABHD11 anticorps (N-Term)

N° du produit ABIN5516391

Cet anticorps Lapin Polyclonal détecte spécifiquement ABHD11 dans WB. Il présente une réactivité envers Humain, Souris, Boeuf (Vache), Chien, Cobaye, Cheval, Lapin, Rat, Saccharomyces cerevisiae et Poisson zèbre (Danio rerio).

Aperçu rapide pour ABHD11 anticorps (N-Term) (ABIN5516391)

Antigène: ABHD11 (Abhydrolase Domain Containing 11 (ABHD11))

Reactivité: Humain, Souris, Boeuf (Vache), Chien, Cobaye, Cheval, Lapin, Rat, Saccharomyces cerevisiae, Poisson zèbre (Danio rerio)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ABHD11 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-ABHD11 anticorps

Épitope: N-Term

Séquence: FNSIAKILAQ QTGRRVLTVD ARNHGDSPHS PDMSYEIMSQ DLQDLLPQLG

Homologie: Cow: 86%, Dog: 93%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 93%, Rat: 100%, Yeast: 92%, Zebrafish: 92%

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

Purification: Affinity purified

Immunogène: The immunogen for Anti-ABHD11 antibody is: synthetic peptide directed towards the N-terminal region of Human ABHDB

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

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.

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 ABHD11

Antigène: ABHD11 (Abhydrolase Domain Containing 11 (ABHD11))

Autre désignation: ABHD11

Sujet: This gene encodes a protein containing an alpha/beta hydrolase fold domain. 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 described, but their biological validity has not been determined.

Alias Symbols: PP1226, WBSCR21

Protein Interaction Partner: SUMO1, UBC, NEDD8, MDM2, APP,

Protein Size: 315

ID gène: 83451

UniProt: Q8NFV4