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About This Item
UNSPSC Code:
12352200
NACRES:
NA.32
Product Name
Cholera Toxin B subunit, recombinant, expressed in HEK 293 cells, subunit A free
recombinant
expressed in HEK 293 cells
assay
≥95% (SDS-PAGE)
form
lyophilized powder
specific activity
(Binds to GM1 ganglioside. The binding EC50 is lower than 1 ug/ml)
mol wt
pentamer observed mol wt ~70 kDa by SDS-PAGE (non-reducing)
calculated mol wt 13 kDa
observed mol wt ~13 & 20 kDa by SDS-PAGE (reducing)
solubility
H2O: soluble 11 mg/mL
UniProt accession no.
storage temp.
−20°C
Quality Level
Related Categories
Analysis Note
Activity measured by ELISA using ganglioside GM1-coated multiwell plates, rabbit anti-Cholera toxin B subunit antibodies, and peroxidase-labeled goat anti-rabbit IgG as the secondary antibody. 50% saturation of binding was achieved with ≤1 μg of Cholera toxin B subunit per mL.
Application
Cholera Toxin B subunit has been used:
- for macrophage stimulation and i.p. injection in a study to determine the endotoxin sensitivity of Caspase-4.
- in transganglionic and retrograde tract-tracing method combined with dual-immunofluorescence histochemistry of adult rat Vmes neuron cells.
General description
The advantage of this product over the native CTXB is that it has no traces of Vibrio cholera, and no contamination of the highly toxic Cholera toxin A subunit. This product is expressed in human HEK 293 cells as a C-terminally his-tagged protein with a calculated molecular mass of 13 kDa (amino acids Thr22-Asn124).
The protein is recombinant, and therefore has no contamination of the highly toxic Cholera toxin A subunit.
Under non-reducing conditions, it migrates as pentamer of ~70 kDa, consistent with the pentamerization of CTXB.
Physical form
Lyophilized from 0.22 μm filtered solution in PBS, pH7.4.
Preparation Note
When reconstituted with water to a final concentration of 1 mg of CTB per ml, the solution will contain 1X PBS
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Si-Yuan Song et al.
Frontiers in neuroanatomy, 14, 600555-600555 (2020-12-18)
This study aimed to investigate the direct monosynaptic projections from cortical functional regions to the cerebrospinal fluid (CSF)-contacting nucleus for understanding the functions of the CSF-contacting nucleus. The Sprague-Dawley rats received cholera toxin B subunit (CB) injections into the CSF-contacting
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