Msx2/Hox8 Antikörper (AA 120-148)

Produktnummer ABIN5534538

Der Kaninchen Polyklonal Anti-Msx2/Hox8-Antikörper wurde für WB validiert. Er ist geeignet, Msx2/Hox8 in Proben von Human zu detektieren.

Kurzübersicht für Msx2/Hox8 Antikörper (AA 120-148) (ABIN5534538)

Target: Msx2/Hox8 (Msx2) (Msh Momeobox 2 (Msx2))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Msx2/Hox8 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-Msx2/Hox8 Antikörper

Bindungsspezifität: AA 120-148

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This MSX2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 120-148 amino acids from the Central region of human MSX2.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: For WB starting dilution is: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Informationen zur Lagerung: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Details zu Msx2/Hox8

Target: Msx2/Hox8 (Msx2) (Msh Momeobox 2 (Msx2))

Andere Bezeichnung: MSX2

Hintergrund: This gene encodes a member of the muscle segment homeobox gene family. The encoded protein is a transcriptional repressor whose normal activity may establish a balance between survival and apoptosis of neural crest-derived cells required for proper craniofacial morphogenesis. The encoded protein may also have a role in promoting cell growth under certain conditions and may be an important target for the RAS signaling pathways. Mutations in this gene are associated with parietal foramina 1 and craniosynostosis type 2.

Molekulargewicht: 29 kDa

Gen-ID: 4488

UniProt: P35548