|Immunogen||Candida albicans, Type A (ATCC #32354).|
|Purification||Protein A chromatography purified IgG fraction covalently coupled with high purity isomer I of fluorescein isothiocyanate. Care is taken to ensure complete removal of any free fluorescein from the final product.|
|Target/Specificity||Recognizes numerous proteins in a soluble C. albicans extract (IEP). Has not been absorbed and does cross-react with other yeasts. Negative against human serum, urine and spinal fluid.|
|Preservative||0.1% Sodium Azide|
|Storage||Short-term (up to 6 months) store at 2-8°C under subdued light. Long term, aliquot and store at -20°C. Avoid multiple freeze/thaw cycles.|
|Precautions||Rabbit Antibody to Candida albicans Fluorescein Conjugated is for research use only and not for use in diagnostic or therapeutic procedures.|
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Provided below are standard protocols that you may find useful for product applications.
The references listed below are for research purposes only:1. Brand, A., et al., (2008), “An Internal Polarity Landmark is Important for Externally Induced Hyphal Behaviors in Candida albicans”, Eukaryotic Cell, 7(4): 712-720.2. Fratti, R.A., et al., (1998), “Endothelial Cell Injury Caused by Candida albicans Is Dependent on Iron”, Infection and Immunity, 66(1): 191-196.3. Tsuchimori, N., et al., (2000), “Reduced Virulence of HWP1-Deficient Mutants of Candida albicans and Their Interactions with Host Cells”, Infection and Immunity, 68(4): 1997-2002.4. Phan, Q.T., et al., (2005), “N-cadherin Mediates Endocytosis of Candida albicans by Endothelial Cells”, The Journal of Biological Chemistry, 280(11): 10455-10461.5. Phan, Q.T., et al., (2000), “Role of Hyphal Formation in Interactions of Candida albicans with Endothelial Cells”, Infection and Immunity, 68(6): 3485-3490.6. Martinez-Lopez, R., et al., (2006), “Candida albicans Ecm33p is Important for Normal Cell Wall Architecture and Interactions with Host Cells”, Eukaryotic Cell., 5(1), 140-147.7. Palmer, G.E., et al., (2005), “The Candida albicans Vacuole is Required for Differentiation and Efficient Macrophage Killing”, Eukaryotic Cell., 4(10), 1677-1686.
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