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Mouse ANG II (Angiotensin II) ELISA Kit

SKU:
AEFI00670
Product Type:
ELISA Kit
Size:
96 Assays
Sensitivity:
18.75pg/ml
Range:
31.25-2000pg/ml
ELISA Type:
Competitive
Reactivity:
Mouse
  • Mouse ANG II (Angiotensin II) ELISA Kit
  • Mouse ANG II (Angiotensin II) ELISA Kit
€599
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Description

Mouse ANG II (Angiotensin II) ELISA Kit

The Mouse Ang II (Angiotensin II) ELISA Kit is a powerful tool for the precise measurement of Angiotensin II levels in mouse serum, plasma, and cell culture supernatants. With excellent sensitivity and specificity, this kit delivers accurate and reproducible results, making it ideal for a wide range of experimental applications.Angiotensin II is a key player in the regulation of blood pressure and fluid balance, exerting its effects through the renin-angiotensin system. Dysregulation of Angiotensin II signaling has been implicated in various cardiovascular diseases, kidney disorders, and metabolic conditions, underscoring its importance as a potential therapeutic target.

By enabling researchers to quantify Angiotensin II levels in biological samples, the Mouse Ang II ELISA Kit facilitates in-depth investigations into the role of this peptide hormone in health and disease. Its reliability and precision make it an invaluable asset for studies aiming to elucidate the mechanisms underlying Angiotensin II-related pathologies and develop novel treatment strategies.

Product Name:Mouse ANG II (Angiotensin II) ELISA Kit
Product Code:AEFI00670
Size:96T
Alias:Angiotensinogen, Serpin A8, Agt
Detection method:Competitive ELISA, Coated with Antigen
Application:ANG II ELISA Kit allows for the in vitro quantitative determination of ANG II concentrations in serum, plasma, tissue homogenates and other biological fluids.
Sensitivity:< 18.75pg/ml
Range:31.25-2000pg/ml
Storage:2-8°C for 6 months
Note:For Research Use Only
Recovery: Matrices listed below were spiked with certain level of ANG II and the recovery rates were calculated by comparing the measured value to the expected amount of ANG II in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)87-9691
EDTA plasma(n=5)85-9991
heparin plasma(n=5)87-10496
Linearity: The linearity of the kit was assayed by testing samples spiked with appropriate concentration of ANG II and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)85-104%91-102%85-100%
EDTA plasma(n=5)87-99%90-98%85-95%
heparin plasma(n=5)87-100%84-100%82-99%
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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