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Rat ADA(Adenosine deaminase) ELISA Kit

SKU:
AEFI00869
Product Type:
ELISA Kit
Size:
96 Assays
Sensitivity:
46.875pg/ml
Range:
78.125-5000pg/ml
ELISA Type:
Sandwich
Reactivity:
Rat
$719
Frequently bought together:

Description

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Rat ADA (Adenosine deaminase) ELISA Kit

The Rat ADA (Adenosine Deaminase) ELISA Kit is a reliable tool for measuring levels of adenosine deaminase in rat serum, plasma, and cell culture supernatants. This kit offers high sensitivity and specificity, ensuring accurate and reproducible results for various research applications.Adenosine deaminase is an important enzyme that plays a key role in purine metabolism and immune function. Abnormal levels of ADA have been linked to various diseases, including immune deficiencies and certain types of cancer.

Therefore, this ELISA kit is a valuable resource for studying the role of ADA in disease pathogenesis and developing potential therapeutic interventions.Overall, the Rat ADA ELISA Kit is a valuable tool for researchers looking to investigate the role of adenosine deaminase in various physiological and pathological processes in rat models.

Product Name:Rat ADA(Adenosine deaminase) ELISA Kit
Product Code:AEFI00869
Size:96T
Alias:Adenosine deaminase, Adenosine aminohydrolase, Ada
Detection method:Sandwich ELISA, Double Antibody
Application:ADA ELISA Kit allows for the in vitro quantitative determination of ADA concentrations in serum, plasma, tissue homogenates and other biological fluids.
Sensitivity:< 46.875pg/ml
Range:78.125-5000pg/ml
Storage:2-8°C for 6 months
Note:For Research Use Only
Recovery: Matrices listed below were spiked with certain level of ADA and the recovery rates were calculated by comparing the measured value to the expected amount of ADA in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)89-10598
EDTA plasma(n=5)91-10499
heparin plasma(n=5)91-10397
Linearity: The linearity of the kit was assayed by testing samples spiked with appropriate concentration of ADA and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)87-104%89-101%87-105%
EDTA plasma(n=5)82-101%84-97%84-100%
heparin plasma(n=5)88-97%80-95%86-100%
CV(%): Intra-Assay: CV<8%
Inter-Assay: CV<10%

When carrying out an ELISA assay it is important to prepare your samples in order to achieve the best possible results. Below we have a list of procedures for the preparation of samples for different sample types.

Sample TypeProtocol
Serum If using serum separator tubes, allow samples to clot for 30 minutes at room temperature. Centrifuge for 10 minutes at 1,000x g. Collect the serum fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.

If serum separator tubes are not being used, allow samples to clot overnight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Remove serum and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.

PlasmaCollect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples at 4°C for 15 mins at 1000 × g within 30 mins of collection. Collect the plasma fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles. Note: Over haemolysed samples are not suitable for use with this kit.
Urine & Cerebrospinal FluidCollect the urine (mid-stream) in a sterile container, centrifuge for 20 mins at 2000-3000 rpm. Remove supernatant and assay immediately. If any precipitation is detected, repeat the centrifugation step. A similar protocol can be used for cerebrospinal fluid.
Cell culture supernatantCollect the cell culture media by pipette, followed by centrifugation at 4°C for 20 mins at 1500 rpm. Collect the clear supernatant and assay immediately.
Cell lysatesSolubilize cells in lysis buffer and allow to sit on ice for 30 minutes. Centrifuge tubes at 14,000 x g for 5 minutes to remove insoluble material. Aliquot the supernatant into a new tube and discard the remaining whole cell extract. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C.
Tissue homogenatesThe preparation of tissue homogenates will vary depending upon tissue type. Rinse tissue with 1X PBS to remove excess blood & homogenize in 20ml of 1X PBS (including protease inhibitors) and store overnight at ≤ -20°C. Two freeze-thaw cycles are required to break the cell membranes. To further disrupt the cell membranes you can sonicate the samples. Centrifuge homogenates for 5 mins at 5000xg. Remove the supernatant and assay immediately or aliquot and store at -20°C or -80°C.
Tissue lysatesRinse tissue with PBS, cut into 1-2 mm pieces, and homogenize with a tissue homogenizer in PBS. Add an equal volume of RIPA buffer containing protease inhibitors and lyse tissues at room temperature for 30 minutes with gentle agitation. Centrifuge to remove debris. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C.
Breast MilkCollect milk samples and centrifuge at 10,000 x g for 60 min at 4°C. Aliquot the supernatant and assay. For long term use, store samples at -80°C. Minimize freeze/thaw cycles.

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