Cholera Toxin Subunit B (Recombinant), Alexa Fluor™ 555 Conjugate
Cholera Toxin Subunit B (Recombinant), Alexa Fluor™ 555 Conjugate
Invitrogen™

Cholera Toxin Subunit B (Recombinant), Alexa Fluor™ 555 Conjugate

Molecular Probes™ cholera toxin conjugates are made from a recombinant version of the B subunit only. This allows us toRead more
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Catalog NumberQuantity
C22843500 μg
C34776100 μg
Catalog number C22843
Price (EUR)
1.292,65
キャンペーン価格
1.418,00
Save 125,35 (9%)
Each
Add to cart
Quantity:
500 μg
Price (EUR)
1.292,65
キャンペーン価格
1.418,00
Save 125,35 (9%)
Each
Add to cart
Molecular Probes™ cholera toxin conjugates are made from a recombinant version of the B subunit only. This allows us to provide a very high-purity product that is completely free of the toxic A subunit. Cholera toxin B subunit (CT-B) attaches to cells by binding to ganglioside GM1, making it a powerful tool for retrograde labeling of neurons. This tracer has been used in a variety of applications, including tracing of rat forebrain afferents, projections of the parabrachial region, and neurons of the urinary bladder wall. When used in neuronal tracing applications, CT-B is typically introduced by pressure injection or by iontophoretic injection into neural tissue.

Cholera Toxin Subunit B Specifications:
• Label (Ex/Em): Alexa Fluor™ 555 (555/565 nm)
• At neutral pH, the 11.4 kDa B subunit exists as a 57 kDa pentamer
• Lyophilized product can be dissolved in buffer (e.g., PBS) for use


Cholera Toxin Subunit B for Studying Lipid Rafts
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 thought to be important in cell signaling. For lipid raft staining, cells are first incubated with fluorescent CT-B. Then, an anti–CT-B antibody is added to crosslink the CT-B in the lipid rafts into distinct patches on the plasma membrane. These patches are easily visualized by fluorescence microscopy. In addition to individual fluorescent CT-B conjugates, we also offer Vybrant™ Lipid Raft Labeling Kits that contain the Alexa Fluor™ 488, Alexa Fluor™ 555, or Alexa Fluor™ 594 dye conjugates of CT-B, an anti–CT-B antibody, and a detailed protocol for labeling and preparing cells for fluorescence microscopy.

Find More CT-B Conjugates
We offer various CT-B conjugates. Review Protein Conjugates—Section 14.7 in the Molecular Probes™ Handbook for more information on these tracers.

For Research Use Only. Not for human or animal therapeutic or diagnostic use.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Label TypeAlexa Fluor Dyes
Product LineAlexa Fluor
Protein FormRecombinant
Protein SubtypeCholera Toxin
Quantity500 μg
Shipping ConditionRoom Temperature
ConjugateAlexa Fluor 555
FormLyophilized
RecombinantRecombinant
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.

Citations & References (27)

Citations & References
Abstract
Autoantigen Golgin-97, an effector of Arl1 GTPase, participates in traffic from the endosome to the trans-golgi network.
Authors:Lu L, Tai G, Hong W
Journal:Mol Biol Cell
PubMed ID:15269279
'The precise cellular function of Arl1 and its effectors, the GRIP domain Golgins, is not resolved, despite our recent understanding that Arl1 regulates the membrane recruitment of these Golgins. In this report, we describe our functional study of Golgin-97. Using a Shiga toxin B fragment (STxB)-based in vitro transport assay, ... More
Caveolin regulates endocytosis of the muscle repair protein, dysferlin.
Authors:Hernández-Deviez DJ, Howes MT, Laval SH, Bushby K, Hancock JF, Parton RG,
Journal:J Biol Chem
PubMed ID:18096699
'Dysferlin and Caveolin-3 are plasma membrane proteins associated with muscular dystrophy. Patients with mutations in the CAV3 gene show dysferlin mislocalization in muscle cells. By utilizing caveolin-null cells, expression of caveolin mutants, and different mutants of dysferlin, we have dissected the site of action of caveolin with respect to dysferlin ... More
Integrin-mediated adhesion regulates membrane order.
Authors:Gaus K, Le Lay S, Balasubramanian N, Schwartz MA
Journal:J Cell Biol
PubMed ID:16943184
'The properties of cholesterol-dependent domains (lipid rafts) in cell membranes have been controversial. Because integrin-mediated cell adhesion and caveolin both regulate trafficking of raft components, we investigated the effects of adhesion and caveolin on membrane order. The fluorescent probe Laurdan and two-photon microscopy revealed that focal adhesions are highly ordered; ... More
Metastatic potential of mouse Lewis lung cancer cells is regulated via ganglioside GM1 by modulating the matrix metalloprotease-9 localization in lipid rafts.
Authors:Zhang Q, Furukawa K, Chen HH, Sakakibara T, Urano T, Furukawa K
Journal:J Biol Chem
PubMed ID:16636068
'To analyze mechanisms for cancer metastasis, we established high metastatic sublines from mouse Lewis lung cancer (P29) by repeated injection. Sublines established from the two subclones H7 and C4 commonly exhibited increased proliferation and invasion activity and reduced expression of ganglioside GM1, although they showed different preferences in their target ... More
Quantitative and dynamic assessment of the contribution of the ER to phagosome formation.
Authors:Touret N, Paroutis P, Terebiznik M, Harrison RE, Trombetta S, Pypaert M, Chow A, Jiang A, Shaw J, Yip C, Moore HP, van der Wel N, Houben D, Peters PJ, de Chastellier C, Mellman I, Grinstein S,
Journal:Cell
PubMed ID:16213220
'Phagosomes were traditionally thought to originate from an invagination and scission of the plasma membrane to form a distinct intracellular vacuole. An alternative model implicating the endoplasmic reticulum (ER) as a major component of nascent and maturing phagosomes was recently proposed (Gagnon et al., 2002). To reconcile these seemingly disparate ... More