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Lamp2

Manufactured by Qiagen
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LAMP2 is a laboratory equipment product offered by Qiagen. It is a device used for the amplification and detection of nucleic acids through the Loop-mediated Isothermal Amplification (LAMP) technique.

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Lab products found in correlation

Cxcl1, by Qiagen (2 mentions) Rneasy plus micro rna isolation kit, by Qiagen (2 mentions) Lamp1, by Qiagen (2 mentions) Brain derived neurotrophic factor (bdnf), by Qiagen (2 mentions) Unc5b, by Qiagen (2 mentions) Efna4, by Qiagen (2 mentions) Efna5, by Qiagen (2 mentions) Cfx384 real time pcr detection system, by Bio-Rad (2 mentions) Nanodrop nd 2000 spectrophotometer, by Thermo Fisher Scientific (2 mentions)

2 protocols using lamp2

1

Quantitative PCR Analysis of Corneal Epithelium

Check if the same lab product or an alternative is used in the 5 most similar protocols
For quantitative polymerase chain reaction (QPCR) studies, epithelium was scraped using a dulled blade and frozen immediately. Four corneas per sample and at least 3 samples per time point were used for the QPCR studies. RNA was extracted using a QIAGEN RNeasy Plus Micro RNA isolation kit (Qiagen) following the manufacturer's protocol. After isolation, the concentration of RNA was quantified using a NanoDrop® ND-2000 Spectrophotometer (Thermo Scientific, Wilmington, DE) and stored at −80 °C until used. QPCR was performed using a Bio-Rad CFX384 Real-Time PCR detection system. The primers used were ordered from Bio Rad, unless otherwise specified: Bec1(qMmuCID0005981), LC3 (qMmuCED0045817), LAMP1 (qMmuCID0027030), LAMP2 (qMmuCID0011408), CXCL1(qMmuCED0047655), BDNF(qMmuCED0050333), NTN1(Qiagen #QT00128478), DCC(Qiagen #QT00135100), Unc5b(Qiagen #QT00167846), Efna4(Qiagen #QT00100681), Efna5(Qiagen #QT00116494), Rgma (Qiagen #QT00310583) and GAPDH (qMmuCED0027497). QPCR data was normalized against GAPDH.
Stepp M.A., Pal-Ghosh S., Tadvalkar G., Williams A., Pflugfelder S.C, & de Paiva C.S. (2018). Reduced intraepithelial corneal nerve density and sensitivity accompany desiccating stress and aging in C57BL/6 mice. Experimental eye research, 169, 91-98.
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2

Quantitative PCR Analysis of Corneal Epithelium

Check if the same lab product or an alternative is used in the 5 most similar protocols
For quantitative polymerase chain reaction (QPCR) studies, epithelium was scraped using a dulled blade and frozen immediately. Four corneas per sample and at least 3 samples per time point were used for the QPCR studies. RNA was extracted using a QIAGEN RNeasy Plus Micro RNA isolation kit (Qiagen) following the manufacturer's protocol. After isolation, the concentration of RNA was quantified using a NanoDrop® ND-2000 Spectrophotometer (Thermo Scientific, Wilmington, DE) and stored at −80 °C until used. QPCR was performed using a Bio-Rad CFX384 Real-Time PCR detection system. The primers used were ordered from Bio Rad, unless otherwise specified: Bec1(qMmuCID0005981), LC3 (qMmuCED0045817), LAMP1 (qMmuCID0027030), LAMP2 (qMmuCID0011408), CXCL1(qMmuCED0047655), BDNF(qMmuCED0050333), NTN1(Qiagen #QT00128478), DCC(Qiagen #QT00135100), Unc5b(Qiagen #QT00167846), Efna4(Qiagen #QT00100681), Efna5(Qiagen #QT00116494), Rgma (Qiagen #QT00310583) and GAPDH (qMmuCED0027497). QPCR data was normalized against GAPDH.
Stepp M.A., Pal-Ghosh S., Tadvalkar G., Williams A., Pflugfelder S.C, & de Paiva C.S. (2018). Reduced intraepithelial corneal nerve density and sensitivity accompany desiccating stress and aging in C57BL/6 mice. Experimental eye research, 169, 91-98.
+ Open protocol
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