FITC antibody (HRP)
Quick Overview for FITC antibody (HRP) (ABIN1099691)
Target
Reactivity
Host
Clonality
Conjugate
Application
Clone
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Specificity
- This antiserum has not been tested for cross-reactivity with other fluorescent compounds.
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Characteristics
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The reactivity of the antiserum is directed to the FITC molecule as tested in direct binding enzyme immunoassay, ELISA and immunoblotting.
IgG concentration is 0.4 mg/mL. Peroxidase/IgG protein molar ratio (E/P) approximately 1.7. No foreign proteins added. -
Immunogen
- Highly purified fluorescein isothiocyanate isomer 1.
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Application Notes
- The optimum working dilution is an assay-related characteristic and should always be determined by titration. For histochemical use optimum dilutions are mostly from 1:100 to 1:500, in ELISA from 1:1,000 upwards, in Western blotting from 1:2,000 upwards. These data should be interpreted as general recommendations only.
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Comment
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Physical form: Horseradish peroxidase conjugated purified mouse IgG1 lyophilized from a solution in phosphate buffered saline (pH 7.2).
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Handling Advice
- The lyophilized product is shipped at ambient temperature and may be stored at +4°C, prolonged storage at or below -20°C. Reconstitute the lyophilized ascites by adding 0.5 ml sterile distilled water. Dilutions may be prepared by adding phosphate buffered saline (PBS, pH 7.2). Avoid repeated thawing and freezing. If a slight precipitation occurs upon storage, this should be removed by centrifugation and will not affect the performance of the product. Diluted solutions should be stored at +4°C, not refrozen, and preferably used the same day.
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Storage
- 4 °C
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- FITC (Fluorescein Isothiocyanate (FITC))
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Alternative Name
- FITC
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Target Type
- Chemical
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Background
- To enhance the specific signal obtained with a monoclonal antibody or a polyclonal second antibody conjugated to FITC. The phenomenon of a weak reaction of a monoclonal antibody is e.g. well known in different analysis of vital peripheral blood mononuclear cells in suspensions by the expression of surface markers. A similar situation exists in solid phase assay systems (ELISA, blotting, DIBA) when used for the identification and /or quantitative determination of minute amounts of soluble specific antigens or antibodies. The sensitivity of the FITC hapten-anti-hapten system makes it a valuable alternative to the biotin- avidin system.
Target
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