霍乱毒素B亚基
  • 供应商:上海索宝生物科技有限公司
  • 联系人:龚思雨
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详细信息

Specifications

General Specifications

Brand:

ALEXA FLUOR® 

Product Size:

100 µg 

Protein Subtype:

Cholera Toxin 

Fluorescence Spectra

Alexa Fluor® 594 goat anti mouse IgG antibody/pH 7.2

Absorption and fluorescence emission spectra of Alexa Fluor® 594 goat anti–mouse IgG antibody in pH 7.2 buffer.

http://probes.invitrogen.com/media/spectra/11005p72.jpg
 
Description
The Alexa Fluor 594 cholera toxin subunit B conjugate is labeled with our bright, photostable, red-fluorescent Alexa Fluor 594 dye (which is spectrally similar to Texas Red dye). The conjugate is derived from nontoxic recombinant B subunit, so it is compley free of the toxic A subunit. Alexa Fluor 594 cholera toxin subunit B conjugate is also available in a unit size of 500 µg (C-22842).

Revised:  02?September?2003
Product Information
Cholera Toxin Subunit B (CT-B) Conjugates
Storage upon receipt:
? ≤ ?20°C
? Desiccate
? Protect from light
Abs/Em:  See Table 1
Introduction
Table 1.  Conjugates of cholera toxin subunit B.
Unit Size  Label  Abs/Em *
100 µg 500 µg
Alexa Fluor 488  495/519  C-34775  C-22841
Alexa Fluor 555  555/565  C-34776  C-22843
Alexa Fluor 594  590/617  C-34777  C-22842
Alexa Fluor 647  650/668  C-34778  
Biotin NA C-34779 
Horseradish
peroxidase (HRP)
NA C-34780 
* Approximate absorption (Abs) and fluorescence emission (Em) maxima, in nm.  NA = Not
applicable. 

Cholera toxin from Vibrio cholerae is comprised of two sub-
units, A and B, arranged in an AB5
 configuration. The A subunit
is an ADP-ribosyltransferase, which disrupts the proper signal-
ing of G proteins and eventually leads to dehydration of the cell.
1
The nontoxic B subunit is important to the protein complex as it
allows the protein to bind to cellular surfaces via the pentasac-
charide chain of ganglioside GM1
.
2
 At neutral pH, the 11.4 kDa
B subunit exists as a 57 kDa pentamer.
3
The B subunit of cholera toxin (CT-B) has proven to be a
powerful tool for retrograde labeling of neurons.
4,5
 This tracer
has been used in a variety of applications, including tracing of ra
forebrain afferents,
6
 projections of the parabrachial region 7
 and
neurons of the urinary bladder wall.
8
 More recently, researchers
have found that CT-B can be used as a marker for lipid rafts,
which are membrane microdomains enriched in cholesterol and
sphingolipids. Lipid rafts segregate specific groups of proteins
and thereby provide a hub for cellular signaling and protein traf-
ficking.
9, 10
Molecular Probes’ CT-B conjugates (Table 1) are made from
recombinant cholera toxin subunit B.  Because the B-subunit
source material is recombinant in origin, it is extremely pure and
compley free of the toxic A subunit.

powder in 0.1 mL or 0.5 mL of buffer, for example, phosphate-
buffered saline (PBS). With the addition of 2 mM sodium azide,
solutions can be stored at 2–6°C for approximay three months.
For longer storage, divide the solution into aliquots and freeze at
≤–20°C.
The peroxidase conjugates of cholera toxin B are supplied in a
unit size of 100 µg. When stored desiccated at –20°C, the lyo-
philized powder is stable for at least six months. Solutions of
1.0 mg/mL can be prepared by dissolving the powder in 0.1 mL
of PBS, pH 7.2. Store solutions at 2–6°C with the addition of
thimerosal to a final concentration of 0.02%. DO NOT USE
AZIDE for the HRP-conjugates. For prolonged storage after re-
constitution, add glycerol to a final concentration of 50% (v/v),
aliquot and store at –20°C. When stored properly, solutions are
stable for approximay three months. PROTECT FROM
LIGHT.  AVOID REPEATED FREEZING AND THAWING OF
SOLUTIONS.
For the Alexa Fluor and biotin conjugates, the lot-specific
degree of labeling (typically 5–10 moles of dye per mole of the
B subunit pentamer) is indicated on the product label.

Product List  Current prices may be obtained from our Web site or from our Customer Service Department.
Cat # Product Name Unit Size
C-34775 cholera toxin subunit B (recombinant), Alexa Fluor? 488 conjugate .......................................................................................... 100 µg
C-22841 cholera toxin subunit B (recombinant), Alexa Fluor? 488 conjugate .......................................................................................... 500 µg
C-34776 cholera toxin subunit B (recombinant), Alexa Fluor? 555 conjugate .......................................................................................... 100 µg
C-22843 cholera toxin subunit B (recombinant), Alexa Fluor? 555 conjugate .......................................................................................... 500 µg
C-34777 cholera toxin subunit B (recombinant), Alexa Fluor? 594 conjugate .......................................................................................... 100 µg
C-22842 cholera toxin subunit B (recombinant), Alexa Fluor? 594 conjugate .......................................................................................... 500 µg
C-34778 cholera toxin subunit B (recombinant), Alexa Fluor? 647 conjugate .......................................................................................... 100 µg
C-34779 cholera toxin subunit B (recombinant), biotin-XX conjugate ....................................................................................................... 100 µg
C-34780 cholera toxin subunit B (recombinant), horseradish peroxidase conjugate ........................................................ ........................ 100 µg

Materials
The biotin- and dye-labeled cholera toxin B subunits are sup-
plied in unit sizes of 100 µg and 500 µg. When stored desiccated
at ≤–20°C, these products are stable for at least six months.
Solutions of 1.0 mg/mL can be prepared by dissolving the

Due to the diversity of applications for the cholera toxin sub-
unit B, please consult the primary literature for appropriate work-
ng concentrations.

References
1. J Biol Chem 255, 1252 (1980);  2.  Mol Microbiol 13, 745 (1994);  3. Biochemistry 35, 16069 (1996);  4. Brain Res 243 215 (1982);  5. Brain Res 231, 33
(1982);  6. Neuroscience 82, 443 (1998);  7. Brain Res 816, 364 (1999);  8. Neuroscience 87, 275 (1998);  9. J Cell Biol 147, 447 (1999);  10. J Cell Biol 141, 929
(1998).