ANTXR2 Antikörper (AA 101-200) (AbBy Fluor® 488)
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- Target Alle ANTXR2 Antikörper anzeigen
- ANTXR2 (Anthrax Toxin Receptor 2 (ANTXR2))
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Bindungsspezifität
- AA 101-200
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser ANTXR2 Antikörper ist konjugiert mit AbBy Fluor® 488
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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
- Top Product
- Discover our top product ANTXR2 Primärantikörper
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- Applikationshinweise
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- 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
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- 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
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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].
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