List of Reagents ・ Ex/Em wavelengths ・ LED light source ・ Filterwork | |
Following are list of most popular reagents we often receive inquiry. Click Spectral button for filterwork guide of each reagent. |
Ex/Em list for other reagents ⇒ |
Notice : | The guide is reference purpose only. It does not guarantee visibility of any certain emission. Result may vary depends on such various factors as LED brightness, filter quality, and camera specifications, etc. |
Symbol Meaning | |
Most suitable | |
* | Most suitable but a long-cut filter may be required to cut the background |
Suitable | |
Usable but with limited effect compared to and | |
Not fit for use |
★ Place pointer above and see LED/Filter wavelengths |
For cellular labeling in fluorescence microscopy and in cell biology. Retains sulfonic acid which is directly connected to the fluorescent. Especially bright with rhodamine derivative. The reagent with great light stability |
|||||||||||||||||
|
||||||||||||||||||
Em/Ex are too close and difficult to separate absorption & excitation spectra. 505nm/SC-56 pair is effective. Filter to cut long wavelength side is required to eliminate background when used with transmitted light source. |
||||||||||||||||||
|
★ Place pointer above and see LED/Filter wavelengths |
In addition to such biological assays as immunocytochemistry, Cyanine dye fluorescence reagent is often used for labelling RNA. |
|||||||||||||||||
|
||||||||||||||||||
Em/Ex are close and difficult to separate absorption & excitation spectra.
505nm & SC-56 pair is effective. Filter to cut long wavelength side is required to eliminate background when used with transmitted light source. |
||||||||||||||||||
|
★ Place pointer above and see LED/Filter wavelengths |
Exhibits strong and stable expression in bacterial cells with minimal toxicity. |
|||||||||||||||||
|
||||||||||||||||||
Em/Ex peaks are close but both lines are spread over wide wavelength and easier to separate. Blue, Cyan, Green LED can be used for excitation and red filter is effective for separation. |
||||||||||||||||||
|
★ Place pointer above and see LED/Filter wavelengths |
The most widely used reagent for band staining. Treated as hazardous waste by many organizations and require special care for handling. | |||||||||||||||||
|
||||||||||||||||||
It has Ex peak at both 300/518nm. LED505/530nm can be used but efficiency is not high. High power light source and effective filter is required to eliminate background. |
||||||||||||||||||
|
|
|
★ Place pointer above and see LED/Filter wavelengths |
A type of fluorochrome widely used for microscopic observation. Often utilized for bloodstain search, dye tracking in the area of forensic medicine and serology |
|||||||||||||||||
|
||||||||||||||||||
Ex peak at 490nm and can be excited with 505nm LED. However Ex/Em is close and may require LED device with background eliminating features. High power blue LED with SC52 filter can also be effective. | ||||||||||||||||||
|
||||||||||||||||||
* 470nm + SC52 pair is also effective |
★ Place pointer above and see LED/Filter wavelengths |
Low cost protein detection with simple protocol. High sensitivity and quantitatively
enables identification of protein by mass spectrometry. Compatible also with UV excitation. |
|||||||||||||||||
|
||||||||||||||||||
Ex 512nm and LED505nm can be effective. LED device with background eliminating
feature or high power blue LED & SC52 pair can also be effective since Ex/Em is close. |
||||||||||||||||||
|
||||||||||||||||||
* 470nm + SC52 pair is also effective |
★ Place pointer above and see LED/Filter wavelengths |
Green fluorescent nucleic acid dye designed to replace the highly toxic EtBr. Compare to EtBr, it is ultra-sensitive and very stable, both hydrologically and thermally. Very simple procedures for pre or post staining | |||||||||||||||||
|
||||||||||||||||||
Wavelength characteristic is similar to FITC, and so is filterworks. | ||||||||||||||||||
|
||||||||||||||||||
* 470nm + SC52 pair is also effective |
★ Place pointer above and see LED/Filter wavelengths |
Fluorescent nucleic acid dye designed to replace the highly toxic EtBr. Compare to EtBr, it is ultra-sensitive and very stable, both hydrologically and thermally. Very simple procedures for pre or post staining. | |||||||||||||||||
|
||||||||||||||||||
Wavelength characteristic is similar to EtBr. Compare to EtBr, it has more abosrption around 520nm and thus LED light is effective. |
||||||||||||||||||
|
★ Place pointer above and see LED/Filter wavelengths |
Enables real time detection without damaging cell. It also demonstrate
its function as fusion protein (GFP tag) Widely used as a tool to locate protein which is taking part in signal transaction inside the cell. |
|||||||||||||||||
|
||||||||||||||||||
Em/Ex peaks are close but Em is spread over to short wavelength side and Blue LED is effective |
||||||||||||||||||
|
★ Place pointer above and see LED/Filter wavelengths |
Red fluorescent proteins isolated from Discosoma sp. Utilizes for fusion expression with target protein, promoter activity monitoring and bacteria expression. Takes short time for expression and stable as well. |
|||||||||||||||||
|
||||||||||||||||||
Em/Ex peaks are close but Em is spread over to short wavelength side and Cyan or Green LED can be used. Excitation with Green LED and separation with red filter is effective. | ||||||||||||||||||
|
★ Place pointer above and see LED/Filter wavelengths |
mCitrine is an empty vector and gene insertion can be achieved by LIC cloning protocol. mCitrine is highly versatile with its compatibility with many other vector as well as usability as single expression vector. | |||||||||||||||||
|
||||||||||||||||||
Ex 510m and 505nm LED is efficient. However Ex/Em is close and may require
LED device with background eliminating features. High power blue LED with
SC52 filter is also effective. |
||||||||||||||||||
|
||||||||||||||||||
* 470nm + SC52 pair is also effective |
★ Place pointer above and see LED/Filter wavelengths |
Ideal Nucleic acid staining reagent for prestained method. Low background and high S/N ratio makes safe alternative to the ethidium bromide. | |||||||||||||||||
|
||||||||||||||||||
Ralatively easy to excite with Blue LED (470m). Easy to separate since Ex/Em peak has some space between them. | ||||||||||||||||||
|
||||||||||||||||||
* SC52 is also effective |
★ Place pointer above and see LED/Filter wavelengths |
||||||||||||||||||
|
||||||||||||||||||
Relatively easy to excite with Blue and Cyan LED. Easy to separate since Ex/Em peak has some space between them. |
||||||||||||||||||
|
★ Place pointer above and see LED/Filter wavelengths |
Asymmetrical cyanine dye used as a nucleic acid stain in molecular biology. It binds to double helix DNA and can be replacement for EtBr as it is safer to work However any small molecule capable of binding DNA with high affinity is a possible carcinogen, including SYBR Green. |
|||||||||||||||||
|
||||||||||||||||||
Ex is similar to SYBR Gold, however Em is adjacent to Ex and bit harder to separate. LED 505 with background eliminating features or high power blue LED & SC52 pair is also effective. |
||||||||||||||||||
|
||||||||||||||||||
* 470nm + SC52 pair is also effective |
★ Place pointer above and see LED/Filter wavelengths |
Provides fast, simple, sensitive staining of proteins. Has very little protein-to-protein variation in staining. Enables long lasting and stable emission. With low background, it requires less time for cleaning gel. Detection with immunoreagent is also possible with western blotting. |
|||||||||||||||||
|
||||||||||||||||||
Ex is spread over to wide range and both Blue and Cyan LED are highly effective for excitation. With enough space between Ex&Em, it is relatively easy to separate too |
||||||||||||||||||
|
★ Place pointer above and see LED/Filter wavelengths |
For cellular labeling in fluorescence microscopy and in cell biology. Retains sulfonic acid which is directly connected to the fluorescent. Especially bright with rhodamine derivative. The reagent with great light stability |
|||||||||||||||||
|
||||||||||||||||||
Ex is spread over to wide range and both blue and cyan are effective for
excitation. Most emission can transmit both SC-56 & SC-60 and it is relatively easy to separate as well. |
||||||||||||||||||
|
★ Place pointer above and see LED/Filter wavelengths |
For cellular labeling in fluorescence microscopy and in cell biology. Retains sulfonic acid which is directly connected to the fluorescent. Especially bright with rhodamine derivative. The reagent with great light stability |
|||||||||||||||||
|
||||||||||||||||||
With wide space between the peaks of Ex & Em, it is considered easy reagent for separation. Blue LED is most effective for excitation. Cyan LED is also effective. |
||||||||||||||||||
|
★ Place pointer above and see LED/Filter wavelengths |
Generated from the wild-type RFP from sea anemone entacmaea quadricolor.
It is brightest monomeric red fluorescent protein available. Mammalian
cells transiently transfected with TagRFP expression vectors produce bright
fluorescence in 10-12 hrs after transfection. |
|||||||||||||||||
|
||||||||||||||||||
Cyan, or Green LED is effective for excitation. Em is too close with Green,
and background may appear with SC-56 but sould be able to separate with SC-60 since Em is spread over to long wavelength side. |
||||||||||||||||||
|
★ Place pointer above and see LED/Filter wavelengths |
Exceptionally bright red fluorescent protein (2.5x brighter than EGFP) It is easily detected as deep as 1 cm below the surface, and ideal for live animal imaging studies. High cohesion stability make it suitable to produce protein N-, C- fusion protein too. | |||||||||||||||||
|
||||||||||||||||||
Wavelength characteristics is similar to Tag RFP and Em/Ex are close. Cyan LED & shortpass filters pair or Green LED & SC-60 filter pair should be used to eliminate background. |
||||||||||||||||||
|
★ Place pointer above and see LED/Filter wavelengths |
YFP is synthetic non-aequorea fluorescent proteins that can be amplified/cut by various PCR and cloned into any other expression vector of choice. These vectors can also be used as expression vectors or as positive controls and allow monitoring of inducible protein expression. | |||||||||||||||||
|
||||||||||||||||||
Ex peak at 512nm and can be excited with 505nm LED. However Ex/Em is close and may require LED device with background eliminating features. High power blue LED with SC52 filter can also be effective. | ||||||||||||||||||
|
||||||||||||||||||
* 470nm + SC52 pair is also effective |
* | ⇒ Long cut filter may required to eliminate background |
Ex/Em list for other reagents ⇒ |
Notice : | The guide is reference purpose only. It does not guarantee visibility of any certain emission. Result may vary depends on such various factors as LED brightness, filter quality, and camera specifications, etc. |