Blueberry leaf mottle virus (BLMoV) ELISA Kit

Name: Blueberry leaf mottle virus (BLMoV) ELISA Kit
SKU: DEIAPV95
Rating: 5 (1 reviews)

Regulatory status: For research use only, not for use in diagnostic procedures.

COA

SDS

Datasheet

Summary

Sample

Host plants

Species Reactivity

Host plants

Detection Method

sELISA

Intended Use

The test can be used to detect BLMV in infected host plants.

Contents of Kit

1. Coating Antibody: 0.25 mL. Specific capture polyclonal antibody (PAb) or monoclonal antibody (MAb) for coating ELISA plate.
2. Detecting Conjugate, alkaline phosphatase: 0.25 mL.
3. ELISA Plate: 5×96T. Empty ELISA plate with high binding capacity. The plate should be used for our ELISA Reagents to achieve a maximum test results.
4. Coating Buffer 10×: 6 mL
5. Sample Buffer: 11.6g
6. Conjugate Buffer 10×: 6 mL
7. PBST Buffer (Powder): 28.7g
8. Tween-20: 7.0g
9. PNP Buffer (5×): 10 mL
10. PNP Tablet: 10 Tablets

Storage

Store all buffers at 2-8°C, except for PNP tablets at -20°C under dark.

Citations

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Documents

pdf COA

pdf SDS

pdf Datasheet

QA & Reviews

Customer Reviews

References

Detection of Viruses and Phytoplasma in Vaccinium sp in the Czech Republic

XXVIII INTERNATIONAL HORTICULTURAL CONGRESS ON SCIENCE AND HORTICULTURE FOR PEOPLE (IHC2010): INTERNATIONAL SYMPOSIUM ON BERRIES: FROM GENOMICS TO SUSTAINABLE PRODUCTION, QUALITY AND HEALTH

Authors: Spak, J.; Pribylova, J.; Kubelkova, D.; Petrzik, K.; Spakova, V.

Abstract

The first survey on the occurrence of viruses and phytoplasma in blueberry Vaccinium corymbosum L. (highbush blueberry) and naturally occurring Vaccinium myrtillus L. was conducted in the Czech Republic in 2005-2010. Plantations, germplasm collections, propagation materials and wild plants were monitored for symptoms, assayed by ELISA kits, for Blueberry scorch virus (BlScV), Blueberry shock virus (BlShV), Blueberry shoestring virus (BSSV), Blueberry leaf mottle virus (BLMoV), Tomato ringspot virus (ToRSV), Tobacco ringspot virus (TRSV) and by PCR for Blueberry red ringspot virus (BRRV) and phytoplasma. In total, 15 locations and 34 cultivars were monitored. Testing for BlScV, BlShV, BSSV, BLMoV, ToRSV, TRSV and phytoplasma was negative. BRRV was detected using primers RRSV3/RRSV4 in 2 plants 'Darrow' at one location.

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