MSX1 anticorps (AA 111-138)

N° du produit ABIN7870112

Cet anticorps Lapin Polyclonal détecte spécifiquement MSX1 dans WB et IF. Il présente une réactivité avec des échantillons de Humain et Souris.

Aperçu rapide pour MSX1 anticorps (AA 111-138) (ABIN7870112)

Antigène: MSX1 (Msh Homeobox 1 (MSX1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MSX1 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Détail du produit anti-MSX1 anticorps

Épitope: AA 111-138

Fonction: MSX1 Antibody

Purification: Antigen affinity purified

Immunogène: A portion of amino acids 111-138 from the human protein was used as the immunogen for the MSX1 antibody.

Isotype: Ig Fraction

Information d'application

Indications d'application: The stated application concentrations are suggested starting points. Titration of the MSX1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % 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.

Stock: -20 °C

Stockage commentaire: Aliquot the MSX1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur MSX1

Antigène: MSX1 (Msh Homeobox 1 (MSX1))

Autre désignation: MSX1

Sujet: Homeobox protein MSX-1 is a member of the muscle segment homeobox gene family. The protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia.

UniProt: P28360

Pathways: Regulation of Muscle Cell Differentiation, Positive Regulation of Response to DNA Damage Stimulus