SCXA anticorps (AA 172-201)

N° du produit ABIN7871263

Cet anticorps anti-SCXA Polyclonal Lapin (ABIN7871263) détecte spécifiquement SCXA dans WB et IHC (p). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour SCXA anticorps (AA 172-201) (ABIN7871263)

Antigène: SCXA (Scleraxis (SCXA))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SCXA est non-conjugé

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

Détail du produit anti-SCXA anticorps

Épitope: AA 172-201

Fonction: SCXA Antibody / Scleraxis

Purification: Antigen affinity

Immunogène: A portion of amino acids 172-201 from the human protein was used as the immunogen for the SCXA antibody.

Isotype: Ig Fraction

Information d'application

Indications d'application: The stated application concentrations are suggested starting points. Titration of the SCXA 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 SCXA antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur SCXA

Antigène: SCXA (Scleraxis (SCXA))

Autre désignation: SCXA

Sujet: Scleraxis/SCXA is a transcription factor that is essential for the proper formation of tendons and ligaments in our bodies. It is responsible for regulating the expression of genes that are involved in tendon development, maintenance, and repair. Without Scleraxis, our tendons and ligaments would not be able to function properly, leading to a host of musculoskeletal issues. Research has shown that mutations in the SCXA gene can lead to conditions such as chronic tendon injuries, tendinopathies, and even developmental abnormalities in tendons.

UniProt: Q7RTU7