- Are lysis buffers, provided in the Proteome Profiler Array kits to prepare cell and/or tissue lysates, interchangeable between kits?
- Lysis buffers packed in the Array Kits are lot matched components and are specific for the lot of Array kits in which they are supplied. For optimal performance of the Array kits, do not interchange or substitute Lysis buffers with those from other lots or sources.
- Are Proteome Profiler™ array results quantitative?
- The Proteome Profiler™ arrays are considered semi-quantitative. Relative levels of protein concentration or phosphorylation are compared between samples by analyzing spot intensity on the array membrane.
- Are tissue lysates a suitable sample type for the Proteome Profiler Arrays?
- A number of the Proteome Profiler Array kits are validated for use with tissue lysates. Please review each kit's manual for validated sample types. If not listed as validated, the kit's compatibility with tissue lysates will need to be determined by the researcher.
- Can a UV transilluminator be used to visualize array signals?
- The use of a UV transilluminator is not recommended to visualize arrays. The recommended methods for visualization are X-ray film, digital image capture systems, and LI-COR (for certain array kits).
- Can Bio-Rad's Chemi Doc be used to image the array membranes?
- Typically, any instrument used to analyze a Western Blot or which can measure chemiluminescence should be compatible with Bio-Techne's array kits. It is possible to image array membranes using a Chemi Doc system as several customers have reported success using this analysis system. Bio-Techne does not have specific recommendations in regards to settings to use, so analysis conditions will need to be optimized by the end user.
- Can ImageJ be used to analyze Proteome Profiler Array images?
- ImageJ can be used to analyze Proteome Profiler Array images. Please contact Bio-Techne Technical Support to request general instructions.
- Can pixel densities associated with experimental samples be normalized to the reference spots or experimental positive controls on the membrane?
- The Array reference spots should not be used for normalization or quantitation primarily because the reference spots consist of unrelated biotinylated proteins spotted at minimal amount directly to the membranes, and the pixel densities of the reference spots are not proportional to the amount of protein loaded on membranes. Experimental signals cannot be normalized to another set of sample data because each antibody may have a different affinity for its respective analyte, which means certain antibody combinations may detect protein at very low pg/mL levels whereas other antibody combinations may require high pg/mL or possibly ng/mL levels for detection. Instead of normalizing data to the reference spots or experimental positive controls, background signal should be subtracted from each analyte spot using the average pixel density from a clear area of the array.
- Can RIPA lysis buffer be used in an Array?
- RIPA buffer is a denaturing lysis buffer. Due to the harsher nature of RIPA on cell membranes and protein interactions, a different profile may be observed when using RIPA buffer instead of the recommended lysis buffer.
- Do frozen serum samples need to be centrifuged after thawing?
- After thawing, serum samples can be used immediately and do not need to be centrifuged.
- Do I need to use the specific protease inhibitors recommended in the insert?
- The specific protease inhibitors are what were used during development and validation of the array. It is recommended to use the same or equivalent inhibitors, or consult the literature or empirically validate the use of other protease inhibitors or cocktails.
- Do Proteome Profiler Arrays cross-react with multiple species?
- Proteome Profiler Arrays have only been tested with the species identified in the kit name. Other species may cross-react with some of the antibodies in the array if there is high homology.Each antibody pair within the kit may have a different level of cross-reactivity.
- Do the Array kits' positive control reference spots produce signals in proportion to the amount of total protein loaded on the membrane?
- The pixel densities of the Arrays' reference spots are not proportional to the amount of protein loaded. The reference spots consist of unrelated biotinylated protein spotted at a minimum amount directly to the membranes for the purpose of confirming the kit detection system works and to assist in aligning the transparency overlay template with the array film or digital image.
- Does Bio-Techne offer multiplex assays with standard curves?
- Bio-Techne offers R&D Systems Luminex Assays and SimplePlex Ella assays. These quantitative assays have validated standard curves and offer multiplex and multianalyte results, respectively. Please contact Technical Service for more information on these product lines.
- Does Lysis Buffer 6 in the Proteome Profiler™ Array contain phosphatase and protease inhibitors?
- Lysis Buffer 6 contains phosphatase inhibitors but not protease inhibitors. If desired, protease inhibitors can be added to the lysis buffer immediately prior to use. We recommend 10 μg/ml Aprotinin (Tocris; Catalog # 4139), 10 μg/ml Leupeptin (Tocris; Catalog # 1167), and 10 μg/ml Peptstatin (Tocris; Catalog # 1190).
- How can the optimal exposure time for analytes on array membranes determined?
- Array kits are designed to detect multiple analytes on a single membrane simultaneously, using different capture and detection antibodies. Each antibody pair has different binding affinity for the target analyte. Additionally, analyte abundance may vary in samples due to multiple factors. Therefore, one exposure time may not be optimal for all the analytes. R&D Systems recommends exposing membranes to X-ray film for 1-10 minutes with multiple exposures to get the best representative signal for low and high abundance analytes.
- How is overexposure of the array membranes defined?
- R&D Systems defines array memebrane overexposure as when the two positive control reference spots merge and appear as a single large spot. Typically, this can be seen when membranes exposure time is > 10 minutes, but overexposure can also be seen earlier depending on other variables.
- How many samples can be analyzed using 1 array kit?
- Most array kits include 4 nitrocellulose membranes per kit. Therefore, four samples can be analyzed per kit. It is recommended to include one control for each expeiment.
- How should adipose tissue lysates be prepared for an Array experiment?
- The tissue lysate preparation protocol provided in the catalog ARY024 product datasheet can be referenced for preparing adipose tissue lysates. Fatty acids and triacylglycerides are not removed after homogenization. Minimal volume of PBS should be added to allow homogenization and produce 100-200 micrograms of lysate protein per array (not tissue weight). Excess PBS will dilute the lysate.
- In the Proteome Profiler Array Kit product datasheets, the materials list references a plastic transparent sheet protector (open on 3 sides). What is an example of what could be used for this?
- Clear plastic sheet protectors can be purchased from office supply stores (e.g., Office Depot, Staples) or found on Amazon. For example, Office Depot Item # 491694 or the Ktrio brand of clear sheet protectors on Amazon are suitable. Clear sheet protectors can be trimmed down to the appropriate size. Please see the Array demo video found here (https://www.rndsystems.com/resources/protocols/profiling-changes-receptor-tyrosine-kinase-phosphorylation-using-antibody-arrays) and fast forward to approximately 6 min 20 sec mark. An example of a plastic sheet protector is shown.
- Is it possible to develop the Arrays using Li-Cor Odyssey system?
- R&D Systems Proteome Profiler Arrays are originally developed for chemiluminscent detection. However, many of the Arrays can be adapted to near-infrared fluorescence detection using the LI-COR Odyssey Infrared Imaging System. To achieve this adaption, the HRP-conjugated Streptavidin provided in the kit is replaced with IRDye 800CW Streptavidin, and the arrays are scanned using a LI-COR Odyssey IIS. Please refer to the protocol: https://www.rndsystems.com/resources/technical/use-proteome-profiler-arrays-li-cor-detection.
- Is there a brand of x-ray film and autoradiography cassettes recommended to use with the array kits?
- Bio-Techne uses Kodak x-ray film (Kodak® BioMax™ Light-1, Catalog # 1788207) or an equivalent. There is no particular brand that is recommended for autoradiography cassettes. What is important is to match the cassette size with the film size. For instance, some cassettes are small and fit only 5 x 7 inch film. Bio-Techne strongly suggests using cassettes that can accommodate 8 x 10 inch film for the flexibility that size provides.
- Should samples be tested in duplicate in a Proteome Profiler Array?
- It is not crucial to run samples in duplicate in a proteome profiler array. Each analyte is spotted in duplicate onto the array membrane allowing for duplicate results per analyte.
- What advantage does a Proteome Profiler Array offer over other sandwich ELISA technologies?
- Proteome Profiler Arrays offer easy and cost-effective analysis of multiple analytes in a simple assay, allowing for identification of trends between and within samples. Arrays use a two site sandwich assay principle but do not require specialized instrumentation.
- What are the dimensions of the array membranes?
- The membranes in our Proteome Profiller Array kits are 6.4 cm long x 2.2 cm wide.
- What image analysis software does Bio-Techne use for the Proteome Profiler Arrays?
- Bio-Techne uses QuickSpots by Ideal Eyes to analyze Proteome Profiler Arrays. QuickSpots and an instructional video on how to use it with R&D Systems Proteome Profiler Arrays can be found at https://idealeyes.com/products/QuickSpots.php.
- What is a transmission mode scanner referenced in the data analysis section?
- A transmission mode scanner referes to any flatbed scanner with a transparency adapter capable of transmission mode. Bio-Techne uses the Epson Perfection V750 PRO scanner.
- What is the sensitivity or minimum detectable amount for each analyte in the array kit?
- It is difficult to define sensitivity for each analyte in an array kit because Proteome Profiler Array is not a quantitative measure of protein expression. Furthermore, sensitivity for a given analyte will differ widely depending on many variables, including sample type, treatment conditions, sample storage and handling, and detection equipment (e.g., film vs digital cameras vs LI-COR, etc.). Arrays measure a difference in relative expression levels of analytes between a control/untreated/healthy sample when compared to an experimental/treated/diseased sample. The individual antibody pairs are optimized to maximize their respective sensitivity while minimizing the cross-reactivity with other analytes on the array.
- What is the spacing of the spots on an array?
- The spots on our arrays are about 1 mm diameter with a center-to-center interval between spots of approximately 2-3 mm, depending on where the spots are in the layout.
- What sample types have been validated with the array kits?
- At a minimum, all array kits have been validated with lysates from ligand-treated cells. In addition, some kits have also been validated with other sample types such as tissue lysates, saliva, milk, urine, serum, plasma, and cell culture supernates. Please consult kit specific product datasheet in the "Sample Collection & Storage" section for details on validated sample types.
- Why do I observe donut/ring formations on the blot rather than a solid dot?
- The donut effect observed in the images is perfectly normal and is related to how the capture antibody dries as part of the printing process. Similar subtle ring effects may be observed in the representative data included in the insert. We recommend measuring the average pixel density across the entire spot instead of doing a point measurement.
- Why might Array and Western blot data conflict?
- It can be challenging to directly compare Western blot and Array data. Arrays detect proteins in their native form while Western Blotting detects linearized and reduced proteins.The Array matrix environment is not optimized for any one analyte, and the antibody pairs may differ in sensitivity, identity, and/or concentration between the applications. To confirm or further quantify Array results, it is recommended to use DuoSet IC ELISAs when available, or another ELISA. In ELISAs, proteins will be in the native form similar to an Array.
- Can the Proteome Profiler™ array membranes be stripped and reused?
- No, Proteome Profiler arrays are validated for single use only. The membranes cannot be stripped and reused.