Dot-Blot sensitivity is significantly reduced if the solution applied to the membrane spreads over a large surface area. Consequently, the samples with low abundance may give false negative results. In many research application it is advantageous to apply sample by capillary action in order to concentrate the sample in a smaller area. There are not many devices currently available for application of multiple samples by capillary action. When processing multiple samples numbering is several hundred, samples are preferably applied on a single membrane in a grid pattern and the resulting membrane containing samples is termed sample array. Devices for making arrays are generally very expensive and complicate to operate. Therefore, there is need for developing a device for making sample arrays that is simple to use and preferably the samples are applied by capillary action.
The present invention relates to a method, a device for application of liquid samples on membrane wherein the sample is applied on the membrane preferably by capillary action. The invention further relates to a method and a device for application of multiple samples on the membrane and creation of sample arrays.
There is provided a device and a method for application of liquid samples on a membrane. The device is such that it allows application of one or more liquid samples on the membrane, preferably by capillary action.
A device for application of liquid samples on a membrane, comprising:
The reservoir open end is connected with the capillary opening with a reservoir-body, wherein the reservoir-body has body circumference or inside diameter wide enough so that when a liquid sample is loaded through the open end the sample may freely migrate (under the force of gravity and without hindrance by surface tension ) down to the capillary opening, i.e., the end opposite the open end. For making such a reservoir, the reservoir-body should have a wide circumference (i.e. internal diameter) which suddenly connect with the capillary opening. Generally a reservoir-body with inside diameter larger than 3–4 mm would allow 1–10 μl liquid samples to freely migrate to the capillary opening. If the reservoir body is narrower it may restrict, due to surface tension, the free migration of small liquid samples, such as 1–10 μl, toward the capillary opening.
The reservoir is either a single reservoir or an assembly of a plurality of individual reservoirs. When there is an assembly of a plurality of individual reservoirs then the reservoirs are spaced from each other such that the open end of the reservoir is compatible with the multi-sample pipetting devices common in the industry. Preferably each individual reservoir is approximately 9 mm apart from the center.
The reservoir-rack is preferably a rectangular shaped plate having one or more through-hole for positioning the reservoir in it. The reservoir may simply be placed in individual through-hole. Preferably, the reservoir-rack allows free up and down movement of the reservoirs. Further, either side or face of the reservoir-rack may be used for positioning the reservoirs. The reservoir-rack may be rotated to 180 degree and/or flipped and placed within the device for use and positioning of the reservoirs.
The assembly of a plurality of the reservoirs in the reservoir-rack is arranged in a grid pattern such that it allows positioning of the reservoirs in columns and rows that meets the application heads of the multi-pipetting devices common in the field and industry, (i.e. multi-channel pipetors).
Preferably each assembly consists of 8 or 12 individual reservoirs. Preferably the reservoir-rack has positions for accommodating at least 96 individual reservoirs or more. Preferably the reservoir-rack is provided with a grid marking for identifying the positions of each reservoir and/or the liquid samples applied on the membrane.
The device assembly is provided with a means (i.e. a frame-means) to secure the membrane for the application of the samples. Further, the device assembly is provided with a base means for positioning the frame-means and a membrane within the frame-means. The reservoir-rack is positioned above the membrane such that when the reservoirs are positioned in the reservoir-rack, the capillary opening of the reservoir contacts or rests on the surface of the membrane. Preferably the device is provided with a non-absorbing surface to be positioned underneath the membrane. Preferably the non-absorbing surface is provided with a soft-surface to crush under pressure, such as a rubber padding.
The capillary opening end of the reservoir is a miro-bore opening, wherein the capillary opening has opening orifice narrow enough to prevent the free flow of the liquid samples out of the reservoir under the force of gravity, and further, the liquid sample only flows out when the capillary opening comes in contact with the surface of the membrane. The capillary opening of the reservoir may be provided with a protruding capillary tip from the reservoir-body. The capillary opening allows flow of the liquid sample from the reservoir into the membrane by capillary action or by applying centrifugal force. The capillary opening may be used for taking aliquots of liquid samples using liquid sampling devices positioned in the open end of the reservoir.
Yet another embedment of the invention comprises a reservoir-rack wherein the reservoir-rack is, preferably, a substantially rectangular shaped plate wherein the positions for the reservoirs are asymmetrically placed such that by rotating (horizontally 180 degree) and/or flipping the reservoir-rack to the opposite side, the positions of the reservoirs or the capillary opening contact on the membrane by the reservoir capillary opening may be changed, providing at least two and a maximum of four alternative points of contact on the membrane below for each reservoir position on the reservoir rack. Thus, the reservoir-rack (and the device) having the potential and the capability to create (closely spaced) one to four points of contact or sample application spots on the membrane below by each reservoir position on the reservoir-rack (and reservoir-capillary opening). The device may be constructed in such way that it matches the footprint of micro-titer plates (an industry standard) and the entire device may be positioned in a centrifuge for spinning the entire device. The device may be constructed of a plastic material or other solid materials.
The invention is further explained with the help of the following drawings.
For using the device, the device is assembled as shown in
Into each reservoir, a small aliquot of a liquid sample (1–20 μl) is deposited through the open end 2. Since the reservoir-body 12 has wide inside diameter (>3 mm), the sample freely migrates and reachs the capillary opening 3, sometime it may be necessary to gently tap the tops plat 11 or the device to facilitate the migration of the liquid sample to the bottom (capillarity opening) of the reservoir. The opening of the capillary end 3 is so narrow that it prevent free flow of the liquid out of the reservoir. When the capillary end of the reservoir contacts with the surface of the membrane, the liquid sample flows out of the reservoir and diffuse into the surface of the membrane by capillary action. Alternatively, the entire device may be placed in a centrifuge and spun, allowing the sample to migrate through the capillary opening 3 and deposit the sample on the membrane opposite the capillary opening 3. For making multiple dots (sample application), the reservoir-rack may be rotated and/or flipped and reposition in the device. (as in
The sample may be loaded into the reservoir by placing a pipetor into the open end 2 of the reservoir and taking an aliquot of the sample through the capillary end 3 of the reservoir. Positioning the reservoir on top of the membrane will allows the sample to diffuse into the membrane by capillary action.
This application claims priority from pending provisional U.S. patent applications Ser. No. 60/229,179 filing date Aug. 28, 2000 and Ser. No. 60/256,732 filing date Dec. 19, 2000.
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3390962 | Herbert | Jul 1968 | A |
4317726 | Shepel | Mar 1982 | A |
4493815 | Fernwood et al. | Jan 1985 | A |
5011779 | Maimon | Apr 1991 | A |
5320811 | Mount et al. | Jun 1994 | A |
6054325 | Kedar et al. | Apr 2000 | A |
6306578 | Schellenberger et al. | Oct 2001 | B1 |
Number | Date | Country | |
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20020023872 A1 | Feb 2002 | US |
Number | Date | Country | |
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60256732 | Dec 2000 | US | |
60229179 | Aug 2000 | US |