產品名稱：LL Rapid Cy3 (3 reactions each up to 200ug)
產    地：Innova Biosciences
產品貨號：340-0010
產品規格：3 x Ab labelings (each 100-200ug scale)
其它產品：
Innova Biosciences 342-0010 3 x Ab labelings (each 100-200ug scale) LL Rapid Cy5 (3 reactions each up to 200ug) 4422
產品說明：
Lightning-Link® Rapid kits
Lightning-Link® Rapid is an innovative technology that enables direct labeling of proteins, peptides or other biomolecules for use in R&D applications, drug discovery and the development of diagnostic kits.
The easy-to-use, one step procedure allows researchers to covalently label biomolecules with only 30 seconds hands on time; furthermore conjugates are ready to use in less than twenty minutes.  The researcher simply pipettes the biomolecule into a vial of lyophilized mixture containing the label of interest and incubates. Despite its apparent simplicity, the Lightning-Link® Rapid process is sophisticated and generates conjugates with performance characteristics identical to, or better than, those prepared with laborious multistep conjugation procedures.
The Lightning-Link® range currently consists of 50+ kits including enzymes, biotin, streptavidin and fluorochromes covering the spectrum from UV to far infrared. Lightning-Link® conjugates are used in a large number of scientific applications including Western Blotting, immunofluorescence, immunohistochemistry, flow cytometry, ELISA and FRET.
Cy3 Label
Cyanine Dye 3 (Cy3) has a strong absorption peak at 550nm and a secondary absorption peak at 520nm. The maximum emission peak is at 570nm, with an excitation coefficient of 1.5 x105 cm-1 M-1. Cy3 can be used as an alternative to Alexa Fluor 555, DY-550, Rhodamine Red-X and TAMRA [5(6)-Carboxytetramethylrhodamine].
Labeled antibodies can be used in many techniques such as flow cytometry, to learn more- please take a look at the Innova webinar "A Beginner's Guide to Flow Cytometry and All You Ever Need to Know About Preparing Fluorescent Conjugated Antibodies".
The technology is fully scalable (μg to grams) ensuring quality and consistency without any deterioration in the performance of the conjugate. As there are no separation or desalting steps, antibody recovery is 100%. Furthermore, the bond between the label and biomolecule is covalent, therefore the conjugate is extremely stable.

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