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[Cloud-Clone] ELISA Kit for WNT1 Inducible Signaling Pathway Protein 2 (WISP2)

관리자 2022.05.02 10:10 조회 850 추천 13
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ELISA Kit for WNT1 Inducible Signaling Pathway Protein 2 (WISP2)

CCN5; CT58; CTGF-L; CCN family member 5; Connective tissue growth factor-like protein; Connective tissue growth factor-related protein 58

  • Product No.SEG894Hu
  • Organism SpeciesHomo sapiens (Human) Same name, Different species.
  • Sample TypeTissue homogenates, cell lysates, cell culture supernates and other biological fluids
  • Test MethodDouble-antibody Sandwich
  • Assay Length3h
  • Detection Range0.312-20ng/mL
  • SensitivityThe minimum detectable dose of this kit is typically less than 0.112ng/mL.
  • DownloadInstruction Manual
  • UOM48T96T 96T*5 96T*10 96T*100
  • FOB



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Specificity

This assay has high sensitivity and excellent specificity for detection of WNT1 Inducible Signaling Pathway Protein 2 (WISP2).
No significant cross-reactivity or interference between WNT1 Inducible Signaling Pathway Protein 2 (WISP2) and analogues was observed.

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level WNT1 Inducible Signaling Pathway Protein 2 (WISP2) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level WNT1 Inducible Signaling Pathway Protein 2 (WISP2) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Stability

The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.



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Reagents and materials provided

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Assay procedure summary

1. Prepare all reagents, samples and standards;
2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;
4. Aspirate and wash 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
6. Aspirate and wash 5 times;
7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
8. Add 50µL Stop Solution. Read at 450nm immediately.



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