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Merck
CN

227040

Anti-Cholera Toxin, B-Subunit Goat pAb

lyophilized, Calbiochem®

别名:

Anti-Cholera Antibody, Cholera Toxin Detection, Goat Anti-Cholera Toxin

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NACRES:
NA.43
UNSPSC Code:
12352203
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产品名称

Anti-Cholera Toxin, B-Subunit Goat pAb, lyophilized, Calbiochem®

biological source

goat

antibody form

serum

antibody product type

primary antibodies

clone

polyclonal

form

lyophilized

contains

≤0.1% sodium azide as preservative

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze

dilution

(Immunoblotting
Frozen Sections (1:4000)
Immunocytochemistry (1:200)
ELISA (1:10,000))

isotype

IgG

shipped in

ambient

storage temp.

2-8°C

target post-translational modification

unmodified

Quality Level

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Application

Immunoblotting (see application references)

Frozen Sections (1:4000; see application references)

Immunocytochemistry (1:200; see application references)

ELISA (1:10,000; see application references)

Disclaimer

Toxicity: Standard Handling (A)

General description

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

Other Notes

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.

Physical form

Undiluted serum.

Preparation Note

Reconstitute in 100 µl dH₂O. Further dilute with aqueous buffers, such as PBS.

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存储类别

11 - Combustible Solids

wgk

WGK 1

法规信息

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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
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
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
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
Mia N Kelly et al.
American journal of physiology. Regulatory, integrative and comparative physiology, 318(6), R1058-R1067 (2020-04-30)
Circadian rhythms are endogenous and entrainable daily patterns of physiology and behavior. Molecular mechanisms underlie circadian rhythms, characterized by an ~24-h pattern of gene expression of core clock genes. Although it has long been known that breathing exhibits circadian rhythms

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