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Rat PMP22 / Peripheral myelin protein 22 ELISA Kit

SKU:
RTFI00347
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
P25094
Sensitivity:
0.094ng/ml
Range:
0.156-10ng/ml
ELISA Type:
Sandwich
Synonyms:
Pmp22, Schwann cell membrane glycoprotein, SAG, Protein CD25, SR13 myelin protein, PMP22, GAS3, PMP-22, GAS-3, Growth arrest-specific protein 3
Reactivity:
Rat
Research Area:
Cell Cycle
€649
Frequently bought together:

Description

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Rat PMP22/Peripheral myelin protein 22 ELISA Kit

The Rat PMP22 (Peripheral Myelin Protein 22) ELISA Kit is specifically designed for the accurate measurement of PMP22 levels in rat serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, ensuring consistent and reliable results for various research applications.PMP22 is a vital protein that plays a key role in peripheral nerve myelination and function. Dysregulation of PMP22 has been linked to peripheral neuropathies such as Charcot-Marie-Tooth disease, making it a valuable biomarker for studying these conditions and researching potential treatment options.

Overall, the Rat PMP22 ELISA Kit provides researchers with a powerful tool for investigating the role of PMP22 in various biological processes and diseases, ultimately leading to a better understanding of peripheral nerve disorders and the development of targeted therapies.

Product Name:Rat Pmp22 (Peripheral myelin protein 22) ELISA Kit
Product Code:RTFI00347
Size:96 Assays
Target:Rat Pmp22
Alias:Pmp22, Schwann cell membrane glycoprotein, SAG, Protein CD25, SR13 myelin protein, PMP22, GAS3, PMP-22, GAS-3, Growth arrest-specific protein 3
Reactivity:Rat
Detection Method:Sandwich ELISA, Double Antibody
Sensitivity:0.094ng/ml
Range:0.156-10ng/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery:Matrices listed below were spiked with certain level of Rat Pmp22 and the recovery rates were calculated by comparing the measured value to the expected amount of Rat Pmp22 in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)85-10092
EDTA plasma(n=5)95-10399
UFH plasma(n=5)87-10595
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Rat Pmp22 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)87-103%87-105%89-104%
EDTA plasma(n=5)87-98%85-100%83-101%
UFH plasma(n=5)80-96%81-92%86-99%
Intra-Assay:CV <8%
Inter-Assay:CV <10%
Uniprot:P25094
UniProt Protein Function:Might be involved in growth regulation, and in myelinization in the peripheral nervous system.
UniProt Code:P25094
NCBI GenInfo Identifier:55904
NCBI Gene ID:
NCBI Accession:CAA44297.1
Molecular Weight:
NCBI Full Name:CD25
UniProt Protein Name:Peripheral myelin protein 22
UniProt Synonym Protein Names:Protein CD25; SR13 myelin protein; Schwann cell membrane glycoprotein; SAG
UniProt Gene Name:Pmp22  
UniProt Entry Name:PMP22_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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