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首页 > 新闻咨询 > 10 种最好的DNA染剂及探针

10 种最好的DNA染剂及探针

Release Time:2020-08-20

Deoxyribonucleic acid (or DNA) is one of the most important macromolecules in biology. It acts as the instructions for critical cell processes such as protein synthesis and is the blueprint for much of cellular structure.

Because of DNA's importance, many visualization and quantification tools have been developed. Reagents and probes have been created to detect DNA in all kinds of applications- microscopy, gel electrophoresis and flow cytometry to name a few.

With over 50 different dyes on the market, it can be a bit overwhelming to determine the optimal one for any given experiment. To simplify the process, here is what we consider the 10 Best DNA Dyes.


Ethidium bromide溴化乙锭

cheap, potential hazard, well-established, impermeable, gel electrophoresis, fluorescence microscopy, orange fluorescence

Ethidium bromide (EtBr) is one of the most popular DNA probes. This is because it was one of the first to be commercially available. As early as the 1950s, it was used to treat diseases in livestock. In the 1970s, scientists began using it as a DNA probe. In addition to its early adoption, ethidium bromide is comparatively inexpensive. Even in large quantities, it remains very affordable, running around $30 per gram.

Ethidium bromide is excellent for staining DNA in agarose gel electrophoresis. It can also be used to detect dsDNA in PCRs.

Upon binding to DNA, EtBr experiences a roughly 20-fold increase in brightness. It releases an orange fluorescence (605 nm) when excited by UV light (~300 nm). Ethidium bromide can also detect RNA depending on how much RNA folding occurs. Ethidium bromide is not a good probe for detecting DNA in live cells, however. This is because it is impermeable to intact cell membranes.

Over the years, health concerns have arisen over ethidium bromide usage. In particular, concerns have been raised about ethidium bromide's role as a mutagen. Ethidium bromide can interfere with DNA replication and transcription in humans when exposed in large quantities. This is due to its properties as an intercalating agent. At low concentrations, however, it is not considered a hazardous waste. This has spurred intense debate as to whether ethidium bromide is optimal for conventional laboratory use.

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Propidium Iodide碘化丙啶

flow cytometry, multiplexing, red fluorescence, 488 nm argon-ion laser, dead cell, impermeable

Propidium iodide is a DNA probe and an intercalating agent. It is in the same chemical family as ethidium bromide. Like ethidium bromide, propidium iodide has a nitrogen-containing ring structure that forms its core. It differs in that it has an additional quaternary amine which binds ionically to an iodide ion.

Upon binding to DNA, propidium iodide will experience a 20-30 fold increase in fluorescence. It can also bind to RNA if folding occurs. Propidium iodide is membrane impermeable. It can only enter cells with compromised membranes. This makes it an excellent probe for identifying dead cells. It can also be used to quantitatively assess DNA content in a biological sample.

Propidium iodide has no sequence preference and binds roughly once per 4-5 base pairs. It can be excited by a xenon- or mercury- lamp as well as a 488 nm argon-ion laser. Because of its emission at 617 nm, it can easily be used in multiplex assays. It can be combined with green fluorescent probes such as fluorescein. It can also be used as a counterstain for multi-color analysis.

In terms of price, it is significantly more expensive than ethidium bromide (about RMB 7000 per gram). However, it is a very common dye for flow cytometry. It can also be used for fluorescence microscopy and fluorescence spectroscopy.

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Crystal Violet结晶紫;龙胆紫

gram stain, gel electrophoresis, non-fluorescent, poor sensitivity, cheap, non-toxic

Crystal violet is a simple chemical compound consisting of three bound benzene rings attached to three amines. It has long been in use for various medical purposes, serving as both an antibacterial agent and a topical antiseptic. It also has a long history of use as a histological stain, with early uses dating back to the late 1800's. Crystal violet is perhaps most well known for its use in Gram staining, to determine if bacteria are gram positive or gram negative.

As a DNA probe, crystal violet can be used for nucleic acid detection in gel electrophoresis. In these applications, it serves as an alternative to fluorescent probes such as ethidium bromide. This is a particularly powerful advantage as use of ultraviolet light sources to excite fluorescent probes may lead to DNA degradation. The tradeoff for such applications of crystal violet, however, is a loss of sensitivity. In experiments, crystal violet has been shown to be less sensitive to DNA than fluorescent probes such as ethidium bromide. Whereas ethidium bromide can detect as little as 1 ng of DNA in a gel band, crystal violet sensitivity sits at around 16 ng. This sensitivity can be improved to 8 ng if a counterstain, such as methyl orange, is used. However, it will still not be as sensitive as ethidium bromide.

In terms of pricing, crystal violet is very affordable. It is also fairly non-toxic. If health concerns are an issue, crystal violet can serve as a non-toxic alternative to some of the more hazardous compounds such as ethidium bromide.

Vendors: BIOFOUNT


dUTP-conjugated Probes

versatile, direct labeling, hybridization, PCR, FISH, DIG-dUTP

dUTP-conjugated probes form an interesting class of DNA detectors mainly resulting from the experimental flexibility they provide. The basic idea is to attach a probe to dUTP with what's called a linker. Then, the dUTP is incorporated into DNA through molecular techniques. This also incorporates the probe into the DNA macromolecule. In this way, the DNA becomes labeled with the probe.

Because dUTP can be conjugated with many different probes, dUTP-conjugates have a wide range of potential applications. For example, dUTP probes can be used to monitor PCR reactions. They can also be used as the probe in FISH procedures. In general, dUTP probes excel in situations where DNA hybridization takes place.

Some of the most common dUTP conjugates include labeling with compounds like digoxigenin (DIG), biotin and fluorescein. Labeling with these compounds all provide non-radioactive probes for DNA detection. These probes in particular have also found widespread use in immunoassays like ELISA.

Vendors:BIOFOUNT


DAPI (4',6-diamidino-2-phenylindole)

blue fluorescence, A-T sequence preference, fluorescence microscopy, slightly permeable, cytotoxic, non-toxic, multiplex

DAPI, like many of the dyes on this list, was first synthesized as a medical agent. It was initially used in an attempt to treat trypanosomiasis, a disease caused by parasites. In the late 1970s, DAPI was adopted for use as a DNA probe due to its efficacy in binding DNA and its large subsequent increase in fluorescence. DAPI binds particularly strongly to A-T rich regions of double-stranded DNA and will experience a roughly 20-fold increase in fluorescence upon binding. It can also bind to RNA, however the fluorescence increase is weaker and the emission is red-shifted.

DAPI is commonly used for fluorescence microscopy. It is particularly successful at staining dead cells or cells with compromised membranes. DAPI can pass through intact cell membranes, albeit with difficulty. Thus, it is not recommended for live cell staining.

DAPI has an excitation of 358 nm and an emission of 461 nm. This means it will appear blue when visualized with a blue/cyan filter. It can also be used in conjunction with green-fluorescent probes such as GFP.

In experiments, DAPI has high cytotoxicity, which reinforces the reason to avoid using DAPI for live cell staining. DAPI is fairly non-toxic to humans if exposure occurs. However, as with many of the DNA probes, it is possible for DAPI to have some mutagenic properties.

Vendors: BIOFOUNT


7-AAD (7-aminoactinomycin D)

G-C sequence preference, multiplexing, red fluorescence, 543 nm helion-neon laser, dead cells, impermeable, fluorescence microscopy, flow cytometry

7-AAD is a fluorescent probe and intercalating agent. Like DAPI, it has a strong affinity for binding double stranded DNA. Unlike DAPI which binds to A-T rich regions, 7-AAD selectively binds to G-C rich regions. It will also bind to RNA, so digestion enzymes may be required before staining.

7-AAD has an excitation of 546 nm and an emission of 647 nm. Because of its large Stokes shift, many researchers use 7-AAD for multi-color analysis in conjunction with blue and green fluorescent probes. 7-AAD is well excited by a 543 nm helium-neon laser.

7-AAD is suitable for use in detecting dead cell populations or cells with compromised membranes. It does not readily pass through intact membranes, making it a poor stain for live cells. 7-AAD has found large use in fluorescence microscopy and flow cytometry.

Vendors: BIOFOUNT


Hoechst 33258 (33342, 34580)

blue fluorescence, live cell, membrane permeable, low cytotoxicity, A-T sequence preference, xenon-mercury lamps, UV laser, fluorescence microscopy, flow cytometry

The Hoechst stains are a group of blue-fluorescent DNA probes. They have been used to stain DNA as early as the 1970s. Developed by the German company Hoechst AG, these dyes offer a good alternative to traditional blue fluorescent dyes.

The Hoechst stains offer significantly greater cell permeability than analogous dyes such as DAPI. This means that Hoechst stains, such as Hoechst 33258, are suitable for staining both live and dead cells. Furthermore, because of the Hoechst dyes' lower cytotoxicity, the impact to live cell populations is greatly reduced.

Hoechst stains will selectively bind to A-T rich regions of double-stranded DNA, specifically binding to the minor groove. Upon binding to DNA, Hoechst stains will undergo an approximately 30-fold increase in fluorescence. The Hoechst stains can be excited by ultraviolet light (~360 nm) and will emit a blue fluorescence (~460 nm). These dyes are compatible with xenon-mercury lamps as well as UV lasers. They are excellent for applications in fluorescence microscopy, immunohistochemistry and flow cytometry.

The difference between Hoechst 33258, 33342 and 34580 are important. Compared to Hoechst 33258, Hoechst 33342 is significantly more permeable due to the addition of a lipophilic ethyl group. For Hoechst 34580, the emission maximum is slightly blue-shifted, residing at 437 nm compared to the 461 nm emission maximum of Hoechst 33258 and Hoechst 33342.

Vendors: BIOFOUNT


PicoGreen®/Helixyte™

high cost, extremely sensitive, green fluorescence, PCR, microplate reader, dsDNA

PicoGreen (and its chemical equivalent Helixyte) is an extremely sensitive probe for double stranded DNA. It can be used for biochemical applications such as quantification of dsDNA in a microplate reader. It can detect as little as 25 ng/mL of dsDNA. This makes it much more sensitive than the Hoechst stains. In addition to its sensitivity, PicoGreen is a very selective probe. It has high affinity for dsDNA over single stranded DNA, RNA and free nucleotides.

PicoGreen, as the name suggests, emits a green fluorescence when bound to DNA. It will also experience a roughly 1000-fold increase in fluorescence. This means it will have a very good signal to noise ratio. It can be used in a variety of applications, such as PCR and micro-array assays. It is a good replacement for DAPI and Hoechst. In particular, it good for when DNA samples are available in limited quantities, thanks to its greater sensitive and selectivity over traditional stains. These advantages come at a price, however. The probe itself is more expensive than traditional stains, costing a few hundred dollars per mL.

Vendors: BIOFOUNT


YOYO®-1/DiYO™-1/TOTO®-1/DiTO™-1

extremely sensitive, high cost, impermeable, flow cytometry, cell viability, cyanine, green fluorescence

These are a family of cyanine dyes based around the compound oxazole yellow. Despite the name however, these dyes actually fluoresce green rather than yellow. For example, YOYO-1 (and its chemical equivalent, DiYO-1) has a maximum emission of 509 nm. The same is true of TOTO-1 (and its chemical equivalent, DiTO-1); this compound has a maximum emission of 535 nm. These compounds are intercalating agents, meaning they will insert themselves between the planar surfaces of DNA base pairs.

This family of DNA probes is particularly well known for its high affinity for DNA. Upon binding to DNA, these probes can experience a one thousand to three thousand fold increase in fluorescence. This strong affinity for DNA makes them excellent for experiments which require great sensitivity. The trade-off though is that these probes are fairly expensive. One mL may cost upwards of a few thousand dollars.

Because these probes are cell-impermeable, they cannot pass through intact cell membranes. They are well suited for staining fixed or dead cells. In this regard, these probes have been commonly used in cell viability and cytotoxicity assays in conjunction with platforms such as flow cytometry.

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SYBR®

green fluorescence, qPCR, gel electrophoresis, high cost, cyanine

SYBR is another family of cyanine based dyes used to stain both DNA and RNA. This family of dyes has high selectivity for double stranded DNA, with lower preference for single stranded DNA and RNA. SYBR dyes are primarily green fluorescent probes (SYBR Green I and SYBR Green II) with the option of yellow fluorescence as well (SYBR Gold).

SYBR dyes have found great use in quantifying DNA. For example, SYBR dyes can be used to monitor quantitative real-time PRC (qPCR). SYBR dyes have also found use in gel electrophoresis. In particular, SYBR dyes have been sold as a safer replacement for the commonly used ethidium bromide. However, evidence is mixed as to whether SYBR dyes are indeed less hazardous than ethidium bromide as both are potential mutagens, stemming from their ability to intercalate with DNA.

In terms of pricing, SYBR dyes are significantly more expensive than ethidium bromide, running about RMB3500 per mL.


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