Rat Peroxiredoxin-2 / PRDX2 ELISA Kit

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SKU:
RTFI00312
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
P35704
Sensitivity:
0.469ng/ml
Range:
0.781-50ng/ml
ELISA Type:
Sandwich ELISA, Double Antibody
Synonyms:
Prdx2, Thioredoxin-dependent peroxide reductase 1, Thioredoxin peroxidase 1, Thiol-specific antioxidant protein, TSA
Reactivity:
Rat
Frequently bought together:

Description

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Product Name:Rat Prdx2 (Peroxiredoxin-2) ELISA Kit
Product Code:RTFI00312
Size:96 Assays
Target:Rat Prdx2
Alias:Prdx2, Thioredoxin-dependent peroxide reductase 1, Thioredoxin peroxidase 1, Thiol-specific antioxidant protein, TSA
Reactivity:Rat
Detection Method:Sandwich ELISA, Double Antibody
Sensitivity:0.469ng/ml
Range:0.781-50ng/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery:Matrices listed below were spiked with certain level of Rat Prdx2 and the recovery rates were calculated by comparing the measured value to the expected amount of Rat Prdx2 in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)89-10194
EDTA plasma(n=5)90-9893
UFH plasma(n=5)89-9994
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Rat Prdx2 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)85-101%86-105%85-101%
EDTA plasma(n=5)82-98%82-96%83-99%
UFH plasma(n=5)86-96%84-100%80-100%
Intra-Assay:CV <8%
Inter-Assay:CV <10%
Uniprot:P35704
UniProt Protein Function:PRDX2: a member of the peroxiredoxin family of antioxidant enzymes, which reduce hydrogen peroxide and alkyl hydroperoxides. Involved in redox regulation of the cell. Reduces peroxides with reducing equivalents provided through the thioredoxin system but not from glutaredoxin. May play an important role in eliminating peroxides generated during metabolism. Might participate in the signaling cascades of growth factors and tumor necrosis factor-alpha by regulating the intracellular concentrations of H(2)O(2). May have a proliferative effect and play a role in cancer development or progression. Three splice-variant isoforms have been identified.
UniProt Protein Details:

Protein type:EC 1.11.1.15; Oxidoreductase

Cellular Component: cytosol; mitochondrion; myelin sheath

Molecular Function:antioxidant activity; peroxidase activity; peroxiredoxin activity; thioredoxin peroxidase activity

Biological Process: activation of MAPK activity; homeostasis of number of cells; hydrogen peroxide catabolic process; hydrogen peroxide metabolic process; inhibition of NF-kappaB transcription factor; negative regulation of lipopolysaccharide-mediated signaling pathway; negative regulation of neuron apoptosis; negative regulation of T cell differentiation; positive regulation of blood coagulation; regulation of apoptosis; regulation of hydrogen peroxide metabolic process; removal of superoxide radicals; respiratory burst during acute inflammatory response; response to lipopolysaccharide; response to oxidative stress; T cell proliferation; thymus development

NCBI Summary:protective enzyme against oxidative damage by cellular reactive sulfur species [RGD, Feb 2006]
UniProt Code:P35704
NCBI GenInfo Identifier:8394432
NCBI Gene ID:29338
NCBI Accession:NP_058865.1
UniProt Secondary Accession:P35704,Q6PDV3,
UniProt Related Accession:P35704
Molecular Weight:21,784 Da
NCBI Full Name:peroxiredoxin-2
NCBI Synonym Full Names:peroxiredoxin 2
NCBI Official Symbol:Prdx2  
NCBI Official Synonym Symbols:Tdpx1  
NCBI Protein Information:peroxiredoxin-2
UniProt Protein Name:Peroxiredoxin-2
UniProt Synonym Protein Names:Thiol-specific antioxidant protein; TSA; Thioredoxin peroxidase 1; Thioredoxin-dependent peroxide reductase 1
Protein Family:Peroxiredoxin
UniProt Gene Name:Prdx2  
UniProt Entry Name:PRDX2_RAT
StepProcedure
1. Set standard, test sample and control (zero) wells on the pre-coated plate respectively, and then, record their positions. It is recommended to measure each standard and sample in duplicate. Wash plate 2 times before adding standard, sample and control (zero) wells!
2.Aliquot 0.1ml standard solutions into the standard wells.
3. Add 0.1 ml of Sample / Standard dilution buffer into the control (zero) well.
4. Add 0.1 ml of properly diluted sample ( Human serum, plasma, tissue homogenates and other biological fluids.) into test sample wells.
5.Seal the plate with a cover and incubate at 37°C for 90 min.
6. Remove the cover and discard the plate content, clap the plate on the absorbent filter papers or other absorbent material. Do NOT let the wells completely dry at any time. Wash plate X2.
7. Add 0.1 ml of Biotin- detection antibody working solution into the above wells (standard, test sample & zero wells). Add the solution at the bottom of each well without touching the side wall.
8.Seal the plate with a cover and incubate at 37°C for 60 min.
9. Remove the cover, and wash plate 3 times with Wash buffer. Let wash buffer rest in wells for 1 min between each wash.
10. Add 0.1 ml of SABC working solution into each well, cover the plate and incubate at 37°C for 30 min.
11. Remove the cover and wash plate 5 times with Wash buffer, and each time let the wash buffer stay in the wells for 1-2 min.
12. Add 90 µL of TMB substrate into each well, cover the plate and incubate at 37°C in dark within 10-20 min. (Note: This incubation time is for reference use only, the optimal time should be determined by end user.) And the shades of blue can be seen in the first 3-4 wells (with most concentrated standard solutions), the other wells show no obvious color.
13. Add 50 µL of Stop solution into each well and mix thoroughly. The color changes into yellow immediately.
14. Read the O.D. absorbance at 450 nm in a microplate reader immediately after adding the stop solution.

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 Type Protocol
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 clotovernight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Removeserum and assay promptly or aliquot and store the samples at-80°C. Avoid multiple freeze-thaw cycles.

Plasma: Collect plasma using EDTA or heparin as an anti-coagulant. 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 Fluid: Collect 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 Supernatant: Collect 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 Lysates: Solubilize 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 Homogenates: The preparation of tissue homogenates will vary depending upon tissue type. Rinse tissue with 1X PBS to remove excess blood & homogenizein 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 Lysates: Rinse 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 Milk: Collect 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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