Product Info Summary
SKU: | EK1607 |
---|---|
Size: | 96 wells/kit, with removable strips. |
Reactive Species: | Rat |
Application: | ELISA |
Sample Types: | cell culture supernatants, cell lysates, serum and plasma (heparin, EDTA). |
Product info
Product Name
Rat TNFRSF19/TROY ELISA Kit PicoKine®
View all TROY/TNFRSF19 ELISA kits
SKU/Catalog Number
EK1607
Size
96 wells/kit, with removable strips.
*Question: How many samples can I assay/run in this kit?
Description
Rat TNFRSF19/TROY ELISA Kit PicoKine® (96 Tests). Quantitate Rat Tnfrsf19 in cell culture supernatants, cell lysates, serum and plasma (heparin, EDTA). Sensitivity: 12pg/ml. The brand Picokine indicates this is a premium quality ELISA kit. Each Picokine kit delivers precise quantification, high sensitivity, and excellent reproducibility. Only our most reliable and effective kits qualify as Picokine, guaranteeing top-tier results for your assays.
Storage & Handling
Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles (Ships with gel ice, can store for up to 3 days in room temperature. Freeze upon receiving.)
Cite This Product
Rat TNFRSF19/TROY ELISA Kit PicoKine® (Boster Biological Technology, Pleasanton CA, USA, Catalog # EK1607)
Clonality of Antibodies
See Datasheet for details
Standard Protein
Expression system for standard: NS0; Immunogen sequence: E30-L170
Sensitivity
<12 pg/ml
Assay Range
62.5 pg/ml - 4,000 pg/ml
Standard Dilution Instructions
See datasheet of EK1607 for more details
Cross-reactivity
There is no detectable cross-reactivity with other relevant proteins.
Reactive Species
EK1607 is reactive to Tnfrsf19 in Rat samples
Validated Sample Types
cell culture supernatants, cell lysates, serum and plasma (heparin, EDTA).
Application Guarantee
EK1607 is guaranteed for ELISA in Rat by Boster Guarantee
See how Boster Bio validate our ELISA kits: ELISA Validation Information
Background of TROY/TNFRSF19
Tumor necrosis factor receptor superfamily, member 19, also known as TNFRSF19 and TROY, is a human gene. It is mapped to 13q12.11-q12.3. The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is highly expressed during embryonic development. It has been shown to interact with TRAF family members, and to activate JNK signaling pathway when overexpressed in cells. This receptor is capable of inducing apoptosis by a caspase-independent mechanism, and it is thought to play an essential role in embryonic development. Alternatively spliced transcript variants encoding distinct isoforms have been described.
Kit Components
Catalog Number | Description | Quantity |
---|---|---|
EK1607-CAP | Anti-Rat Tnfrsf19 Pre-coated 96-well strip microplate | 1 |
EK1607-ST | Rat Tnfrsf19 Standard | 2 vials, 10 ng/tube |
EK1607-DA | Rat Tnfrsf19 Biotinylated antibody (100x) | 100ul |
AR1103 | Avidin-Biotin-Peroxidase Complex (100x) | 100ul |
AR1106-1 | Sample Diluent | 30ml |
AR1106-2 | Antibody Diluent | 12ml |
AR1106-3 | Avidin-Biotin-Peroxidase Diluent | 12ml |
AR1104 | Color Developing Reagent (TMB) | 10ml |
AR1105 | Stop Solution | 10ml |
AR1106-5 | Wash Buffer (25x) | 20ml |
PLA-SEA | Adhesive plate sealers | 4 |
*The kit components are not available for individual purchase.
Materials Required But Not Included In Kit
- Microplate Reader capable of reading absorbance at 450nm.
- Incubator.
- Automated plate washer (optional).
- Pipettes and pipette tips capable of precisely dispensing 0.5 µl through 1 ml volumes of aqueous solutions.
- Multichannel pipettes are recommended for large amount of samples.
- Deionized or distilled water.
- 500ml graduated cylinders.
- Test tubes for dilution.
Data Examples, Quality Control Data & Sample Dilution
Validation Standard Curve O.D. At 450nm
Concentration (pg/ml) | 0 | 62.5 | 125 | 250 | 500 | 1000 | 2000 | 4000 | |
O.D. | 0.007 | 0.101 | 0.216 | 0.375 | 0.759 | 1.302 | 1.832 | 2.03 |
Data Example Images
Click image to see more details
Rat TNFRSF19/TROY PicoKine ELISA Kit standard curve
Recommended Sample Dilution Ratios
According to our internal validation assays using this ELISA kit, to detect TROY/TNFRSF19, Dilution ratio of 1:1, concentration in serum and plasma is around 250 pg/ml..
Intra Assay Consistency & Inter Assay Consistency
We measured random samples of Rat TNFRSF19/TROY ELISA Kit PicoKine® within the same batch/lot to ensure the consistency of the kits' performances. ELISA intra assay consistency is measured using wells from the same plate/assay kit. ELISA inter assay consistency is measured using wells from different plates from the same batch production/lot.
Intra-Assay Precision | Inter-Assay Precision | |||||
---|---|---|---|---|---|---|
Sample | 1 | 2 | 3 | 1 | 2 | 3 |
n | 16 | 16 | 16 | 24 | 24 | 24 |
Mean (pg/ml) | 161 | 625 | 1725 | 161 | 663 | 1839 |
Standard deviation | 11.75 | 33.12 | 115.57 | 13.84 | 43.09 | 156.5%1 |
CV (%) | 7.3% | 5.3% | 6.7% | 8.6% | 6.5% | 8.5% |
Reproducibility
We ensure reproducibility by testing three samples with differing concentrations of TROY/TNFRSF19 in ELISA kits from four different production batches/lots.
Lots | Lot 1 (pg/ml) | Lot 2 (pg/ml) | Lot 3 (pg/ml) | Lot 4 (pg/ml) | Mean (pg/ml) | Standard Deviation | CV (%) |
---|---|---|---|---|---|---|---|
Sample 1 | 161 | 158 | 157 | 156 | 158 | 1.87 | 1.1% |
Sample 2 | 625 | 573 | 633 | 566 | 599 | 29.98 | 5% |
Sample 3 | 1725 | 1554 | 1742 | 1569 | 1647 | 86.37 | 5.2% |
Protein Target Info & Infographic
Gene/Protein Information For Tnfrsf19 (Source: Uniprot.Org, NCBI)
Gene Name
Tnfrsf19
Full Name
Tumor necrosis factor receptor superfamily member 19
Weight
45288 MW
Alternative Names
Protein Tnfrsf19 ;Tnfrsf19 ; Tnfrsf19|AL023044, AW123854, TA, TAJ, TAJ-, TAJ-ALPHA, TRA, TRADE, Tr, Troy|tumor necrosis factor receptor superfamily, member 19|tumor necrosis factor receptor superfamily member 19|Toxicity and JNK inducer
*if product is indicated to react with multiple species, protein info is based on the gene entry specified above in "species".For more info on Tnfrsf19, check out the Tnfrsf19 Infographic
We have 30,000+ of these available, one for each gene! check them out.
In this infographic you will see the following information for Tnfrsf19: database IDs, super-family, protein function, synonyms, molecular weight, chromosomal locations, tissues of expression, subcellular locations, post translational modifications, and related diseases, research areas & pathways. If you want to see more information included, or would like to contribute to it and be acknowledged, please contact us [email protected].
Specific Publications For Rat TNFRSF19/TROY ELISA Kit PicoKine® (EK1607)
Hello CJ!
EK1607 has been cited in 1 publications:
*The publications in this section are manually curated by our staff scientists. They may differ from Bioz's machine gathered results. Both are accurate. If you find a publication citing this product but is missing from this list, please let us know we will issue you a thank-you coupon.
Multifunctional Compound AD-35 Improves Cognitive Impairment and Attenuates the Production of TNF-α and IL-1β in an Aβ 25–35-induced Rat Model of Alzheimer’s Disease
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Customer Reviews
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Customer Q&As
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Find answers in Q&As, reviews.
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10 Customer Q&As for Rat TNFRSF19/TROY ELISA Kit PicoKine®
Question
Q: Can TROY ELISA Kits be used with tissue homogenates (or other non-validated sample types)?
H. Bhasin
Verified customer
Asked: 2020-11-25
Answer
A: Unfortunately, Boster Bio has not routinely validated tissue homogenates as a sample type for ELISA kits. This does not mean that ELISA kits are not suitable for other sample types than we have tested: it means further investigation is required. One will need to perform a spike and recovery study to determine if an unvalidated sample type will work with a particular kit. To perform a spike and recovery experiment, one should divide a sample into two aliquots. In one of the aliquots, the user should spike in a known amount of the kit standard. a dilution series is performed comparing the spiked versus the unspiked sample. Generally, samples with expected recovery and linearity between 80-120% are considered acceptable. This method can be used to validate any sample type that has not been evaluated by Boster Bio. for a more detailed spike and recovery protocol, please contact technical support.
Note: acceptable ranges should be determined individually by each laboratory. Additionally, technical support can help determine if a buffer component is not compatible with a given ELISA kit. please view the Citations tab on the product webpage for peer-reviewed papers utilizing a wide range of sample types. We also have an innovator's reward program where if the user validates our ELISA kits in applications or samples previously not validated by Boster Bio or other users, and share such information with us by submit a review, we will reward the user's efforts with a free antibody or ELISA kit from our catalog. Biocompare.com will also give $20 Amazon giftcard as an additional reward, if the review is submitted there as well.
Boster Scientific Support
Answered: 2020-11-25
Question
Q: Are Boster Bio recombinant proteins and antibodies sterile?
Verified Customer
Verified customer
Asked: 2020-11-08
Answer
A: although the vials are bottled using aseptic techniques, heat-treated vials, and sterile stock solutions, they are not considered or guaranteed to be sterile. If sterile material is needed for an experiment, the material can be filtered through a 0.2 micron filter designed for use with biological fluids.
Boster Scientific Support
Answered: 2020-11-08
Question
Q: What is the optimal O.D. value for TROY ELISA kit? I performed your TROY ELISA on serum samples. For my positive control, I received an O.D. value of 0.826, while my negative control received a value of 0.136. I obtained both of these controls from the ELISA kit, where your kit's typical data shows O.D. values much higher than my positive control and your background is lower. My samples O.D. values are around 0.225 and the highest is only 0.357. can I consider these samples contain TROY even though the O.D. values are not very high?
S. Collins
Verified customer
Asked: 2020-03-30
Answer
A: The absolute O.D. values may change according to incubation time. The more you incubate the higher the O.D. values are going to be. a point of focus should be is whether your sample O.D. values are statistically significantly higher than your blank values. regarding your assay, you could extend your development time in the substrate incubation step to obtain higher O.D. values, as long as your negative controls' O.D. values are not increasing faster in proportion to your positive controls. normally, a sample with O.D. value 2 standard deviations higher than your negative controls can be considered positive. We calculate the sensitivity of this ELISA kit by changeing cutoff O.D. value, calculated as the average of 20 negative controls plus 2 standard deviations of the 20 negative controls, into a concentration. in other words, when we claim this TROY ELISA kit to have sensitivity of 12pg/ml, that means the minimum amount of TROY that can be declared/interpreted as positive by the above standard is 12pg/ml.
Boster Scientific Support
Answered: 2020-03-30
Question
Q: can you tell me how to prepare cell lysates prepared for use in Picokine® ELISA kits?
W. Zhou
Verified customer
Asked: 2019-12-20
Answer
A: for those Picokine® ELISAs where cell or tissue lysate is a validated sample type, sample preparation instructions for lysate can be found in the product insert. Components in lysate and lysis buffer can affect immunoreactivity, so if lysate is not a validated sample type, care must be taken in sample preparation and validation.
Boster Scientific Support
Answered: 2019-12-20
Question
Q: how to analyze ELISA data? I measured TROY level in serum.
L. Campbell
Verified customer
Asked: 2019-11-30
Answer
A: please read this article on ELISA data analysis. bosterbio.com/ELISA-data-analysis-instructions. we also provide a convenient online tool that you can use to analyze ELISA data. bosterbio.com/biology-research-tools/ELISA-data-analysis-online
Boster Scientific Support
Answered: 2019-11-30
Question
Q: how to thaw whole blood sample for TROY ELISA after freezing?
Verified Customer
Verified customer
Asked: 2019-03-23
Answer
A: do not freeze and thaw whole blood. erythrocytes are fragile and, if frozen and thawed, will undergo hemolysis rendering the samples useless. To keep your blood samples to test TROY for a later time, you should let the blood clot in glass tubes and separate the serum to freeze for later analysis.
Boster Scientific Support
Answered: 2019-03-23
Question
Q: we need your suggestion regarding the dilution ratio of serum samples for detection of TROY in Rat serum? I am trying to measure a few analytes and it requires 100ul of diluted samples for each well. We have limited sample volumes so we like to dilute as much as possible.
Verified Customer
Verified customer
Asked: 2018-10-19
Answer
A: without having an understanding the physiological or pathological context of your samples we cannot recommend a dilution ratio without performing a pilot test with your samples. Here is how you can perform a pilot study on your own: perform a serial dilution of your samples on the TROY ELISA kit to make sure you have a linear ascending curve followed by a plateau, which signifies the samples saturating the detection limit of the kit. Then you can pick the dilution ratios from samples in the linear part of the curve as your experimental dilution ratio.
If you are interested in using our ELISA service, you can also send us your sample and we will take care of everything for you. You can check our service details here: bosterbio.com/services/assay-services/ELISA-testing-service
Since you mentioned you have limited samples, our cost effective multiplex ELISA service would fit perfectly for your needs, where we can generate dozens of data points using as little as 25ul sample volume. Information on this service is also in the above link.
Boster Scientific Support
Answered: 2018-10-19
Question
Q: if the enzyme conjugated TROY antibodies are mixed with the substrate, will that convert the substrate into the enzymatic reaction product? Or the enzyme function is only activated when the antibody is attached with the TROY antigen?
D. Zhao
Verified customer
Asked: 2018-09-28
Answer
A: The enzyme is always active. Avoid contaminating the substrate with enzyme prior to the incubation otherwise it compromises the assay with false positive signal.
Boster Scientific Support
Answered: 2018-09-28
Question
Q: is it okay to use citrate plasma as samples in Rat TROY Picokine® ELISA Kit (Catalog # EK1607)?
W. Lewis
Verified customer
Asked: 2018-07-09
Answer
A: Chelating agents such as EDTA, Heparin and Citrate can bind metal ions from the functional domain of TROY causing disruption of its protein structure. TROY may be denatured as a result and may compromise the assay's measurements. The chilating sites could also be too close to the epitopes needed for detection and block the antigen antibody reaction. We have tested the TROY ELISA, treating samples with different anticoagulants and decided that heparin or EDTA can be used for treatment of blood/plasma samples. Do not use other anticoagulents when collecting samples.
Boster Scientific Support
Answered: 2018-07-09
Question
Q: for how much duration can samples (cell cultures, serum, and plasma) be stored and still be stable for measuring TROY using the EK1607 Rat TROY Picokine® ELISA Kit?
B. Krishna
Verified customer
Asked: 2014-11-14
Answer
A: Boster Bio does not assess sample stability. Variations in sample collection, processing, and storage may affect the stabilityof samples. It is recommend to assay sample right after collection when possible, or aliquot into single use volumes and store samples frozen. limit repetitive freeze-thaw cycles with the stored samples to prevent protein degradation.
Boster Scientific Support
Answered: 2014-11-14