ANTXR2 Antikörper (AA 101-200) (Alexa Fluor 647)

Produktnummer ABIN1389096

Produktdetails anti-ANTXR2 Antikörper (Alexa Fluor 647)

Target: ANTXR2 (Anthrax Toxin Receptor 2 (ANTXR2))

Bindungsspezifität: AA 101-200

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ANTXR2 Antikörper ist konjugiert mit Alexa Fluor 647

Applikation: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Homologie: Human,Mouse,Rat,Dog,Cow,Pig,Horse,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human ANTXR2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu ANTXR2

Target: ANTXR2 (Anthrax Toxin Receptor 2 (ANTXR2))

Andere Bezeichnung: ANTXR2 (ANTXR2 Produkte)

Synonyme: CMG-2 antikoerper, CMG2 antikoerper, HFS antikoerper, ISH antikoerper, JHF antikoerper, 2310046B19Rik antikoerper, AW561899 antikoerper, cI-35 antikoerper, ANTXR2 antikoerper, DKFZp459A152 antikoerper, si:ch211-116k3.1 antikoerper, anthrax toxin receptor 2 antikoerper, anthrax toxin receptor 2a antikoerper, ANTXR2 antikoerper, Antxr2 antikoerper, antxr2 antikoerper, antxr2a antikoerper

Hintergrund:

Synonyms: CMG2, ISH, JHF, anthrax toxin receptor 2, ANTR2_HUMAN, Antxr2, Capillary morphogenesis gene 2 protein, CMG 2, CMG-2.

Background: This gene encodes a receptor for anthrax toxin. The protein binds to collagen IV and laminin, suggesting that it may be involved in extracellular matrix adhesion. Mutations in this gene cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009].