227040
Anti-Cholera Toxin, B-Subunit Goat pAb
lyophilized, Calbiochem®
Synonym(e):
Anti-Cholera Antibody, Cholera Toxin Detection, Goat Anti-Cholera Toxin
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Alle Fotos(1)
About This Item
UNSPSC-Code:
12352203
NACRES:
NA.43
Empfohlene Produkte
Biologische Quelle
goat
Qualitätsniveau
Antikörperform
serum
Antikörper-Produkttyp
primary antibodies
Klon
polyclonal
Form
lyophilized
Enthält
≤0.1% sodium azide as preservative
Hersteller/Markenname
Calbiochem®
Lagerbedingungen
OK to freeze
Isotyp
IgG
Versandbedingung
ambient
Lagertemp.
2-8°C
Posttranslationale Modifikation Target
unmodified
Allgemeine Beschreibung
Goat polyclonal antibody supplied as lyophilized undiluted serum. Recognizes cholera toxin B-subunit.
Recognizes the B-subunit of cholera toxin.
This Anti-Cholera Toxin, B-Subunit Goat pAb is validated for use in Immunoblotting, Frozen Sections, Immunocytochemistry, ELISA for the detection of Cholera Toxin, B-Subunit.
Immunogen
Vibrio cholerae
non-denatured Cholera Toxin, B-subunit
Anwendung
Immunoblotting (see application references)
Frozen Sections (1:4000; see application references)
Immunocytochemistry (1:200; see application references)
ELISA (1:10,000; see application references)
Frozen Sections (1:4000; see application references)
Immunocytochemistry (1:200; see application references)
ELISA (1:10,000; see application references)
Warnhinweis
Toxicity: Standard Handling (A)
Physikalische Form
Undiluted serum.
Rekonstituierung
Reconstitute in 100 µl dH₂O. Further dilute with aqueous buffers, such as PBS.
Sonstige Hinweise
Antibody should be titrated for optimal results in individual systems.
Vadolas, J., et al. 1995. Eur. J. Immunol. 25, 969.
Craig, J.P. 1971. Microbial Toxins 2A, 189.
Selected Citations
Peters, I., et al. 2009. Biochim. Biophys. Acta1788, 964.
Balasubramanian, N., et al. 2007. Nature Cell Biology9, 1381.
Nemchinov, L.G., Et al. 2000. Arch. Virol.145, 2557.
Craig, J.P. 1971. Microbial Toxins 2A, 189.
Selected Citations
Peters, I., et al. 2009. Biochim. Biophys. Acta1788, 964.
Balasubramanian, N., et al. 2007. Nature Cell Biology9, 1381.
Nemchinov, L.G., Et al. 2000. Arch. Virol.145, 2557.
Rechtliche Hinweise
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
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Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 1
Analysenzertifikate (COA)
Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.
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Nagaraj Balasubramanian et al.
Nature cell biology, 9(12), 1381-1391 (2007-11-21)
Integrin-mediated adhesion regulates membrane binding sites for Rac1 within lipid rafts. Detachment of cells from the substratum triggers the clearance of rafts from the plasma membrane through caveolin-dependent internalization. The small GTPase Arf6 and microtubules also regulate Rac-dependent cell spreading
L G Nemchinov et al.
Archives of virology, 145(12), 2557-2573 (2001-02-24)
Hepatitis C virus (HCV) is a major cause of acute and chronic hepatitis with over 180 million cases worldwide. Vaccine development for HCV has been difficult. Presently, the virus cannot be grown in tissue culture and there is no vaccine
Jing Du et al.
Cerebrospinal fluid research, 6, 3-3 (2009-03-19)
It has been shown that distal cerebrospinal fluid-contacting neurons (dCSF-CNs) exist near the ventral midline of the midbrain aqueduct and also in the grey matter of the inferior third ventricle and the fourth ventricle floor in the superior segment of
Abir Maarouf Kabbani et al.
Proceedings of the National Academy of Sciences of the United States of America, 117(26), 14978-14986 (2020-06-20)
AB5 bacterial toxins and polyomaviruses induce membrane curvature as a mechanism to facilitate their entry into host cells. How membrane bending is accomplished is not yet fully understood but has been linked to the simultaneous binding of the pentameric B
J Müthing et al.
Glycoconjugate journal, 14(1), 19-28 (1997-01-01)
In this study the comparative TLC immunostaining investigation of neutral GSLs and gangliosides from human skeletal and heart muscle is described. A panel of specific polyclonal and monoclonal antibodies as well as the GM1-specific choleragenoid were used for the overlay
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