SCXA Antikörper (AA 172-201)

Produktnummer ABIN7871263

Der Kaninchen Polyklonal anti-SCXA Antikörper (ABIN7871263) detektiert spezifisch SCXA in WB und IHC (p). Dieser Antikörper reagiert spezifisch mit Proben aus Human.

Kurzübersicht für SCXA Antikörper (AA 172-201) (ABIN7871263)

Target: SCXA (Scleraxis (SCXA))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SCXA Antikörper ist unkonjugiert

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

Produktdetails anti-SCXA Antikörper

Bindungsspezifität: AA 172-201

Verwendungszweck: SCXA Antibody / Scleraxis

Aufreinigung: Antigen affinity

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

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: 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.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Aliquot the SCXA antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Details zu SCXA

Target: SCXA (Scleraxis (SCXA))

Andere Bezeichnung: SCXA

Hintergrund: 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