lbpa standard (Echelon Biosciences)


Structured Review
![A: HeLa cells were labeled with [32P]Pi for 24 h, chased for 14 h, and then treated or not with 0.7 mM HPCD (as in Fig. 1). Lipids were extracted, separated by 2D-TLC, and visualized by autoradiography. The position of <t>LBPA</t> (arrow) was identified <t>by</t> <t>comigration</t> with pure synthetic LBPA as standard. Right: LBPA quantified in 2D-TLCs at different time after HPCD treatment and expressed as a percentage of total 32P-phospholipids (PL). B: Cells labeled as in A were treated or not with 0.7 mM HPCD for 1 h. The lipids were extracted from medium and separated by 2D-TLC. Right shows the quantification of LBPA and total phospholipids in medium. Data are expressed as a percentage of total cellular LBPA or phospholipids, extracted, and quantified in the same experiments.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_6697/pmc06446697/pmc06446697__832fig2.jpg)
Lbpa Standard, supplied by Echelon Biosciences, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/lbpa standard/product/Echelon Biosciences
Average 91 stars, based on 1 article reviews
Price from $9.99 to $1999.99
Images
1) Product Images from "Cyclodextrin triggers MCOLN1-dependent endo-lysosome secretion in Niemann-Pick type C cells"
Article Title: Cyclodextrin triggers MCOLN1-dependent endo-lysosome secretion in Niemann-Pick type C cells
Journal: Journal of Lipid Research
doi: 10.1194/jlr.M089979
![... 2D-TLC, and visualized by autoradiography. The position of LBPA (arrow) was identified by comigration with pure synthetic ... A: HeLa cells were labeled with [32P]Pi for 24 h, chased for 14 h, and then treated or not with 0.7 mM HPCD (as in Fig. 1). Lipids were extracted, separated by 2D-TLC, and visualized by autoradiography. The position of LBPA (arrow) was identified by comigration with pure synthetic LBPA as standard. Right: LBPA quantified in 2D-TLCs at different time after HPCD treatment and expressed as a percentage of total 32P-phospholipids (PL). B: Cells labeled as in A were treated or not with 0.7 mM HPCD for 1 h. The lipids were extracted from medium and separated by 2D-TLC. Right shows the quantification of LBPA and total phospholipids in medium. Data are expressed as a percentage of total cellular LBPA or phospholipids, extracted, and quantified in the same experiments.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_6697/pmc06446697/pmc06446697__832fig2.jpg)
Figure Legend Snippet: A: HeLa cells were labeled with [32P]Pi for 24 h, chased for 14 h, and then treated or not with 0.7 mM HPCD (as in Fig. 1). Lipids were extracted, separated by 2D-TLC, and visualized by autoradiography. The position of LBPA (arrow) was identified by comigration with pure synthetic LBPA as standard. Right: LBPA quantified in 2D-TLCs at different time after HPCD treatment and expressed as a percentage of total 32P-phospholipids (PL). B: Cells labeled as in A were treated or not with 0.7 mM HPCD for 1 h. The lipids were extracted from medium and separated by 2D-TLC. Right shows the quantification of LBPA and total phospholipids in medium. Data are expressed as a percentage of total cellular LBPA or phospholipids, extracted, and quantified in the same experiments.
Techniques Used: Labeling, Autoradiography