Human PPIF (Cyclophilin F) knockout HEK-293T cell lysate
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PPIF KO cell lysate available now. KO validated by Western blot. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, Homozygous: 1 bp insertion in exon 1.
View Alternative Names
CYP3, CyP-D, CyP-M, Cyclophilin 3, Cyclophilin D, Cyclophilin F, Mitochondrial cyclophilin, PPIF_HUMAN, PPIase, PPIase F, Peptidyl prolyl cis trans isomerase, mitochondral, Peptidyl-prolyl cis-trans isomerase F, Peptidyl-prolyl cis-trans isomerase F, mitochondrial, Peptidylprolyl isomerase F, Peptidylprolyl isomerase F (cyclophilin F), Rotamase, Rotamase F, hCyP3, mitochondrial
- WB
Lab
Western blot - Human PPIF (Cyclophilin F) knockout HEK-293T cell lysate (AB257039)
Lane 1 : Wild-type HEK-293T cell lysate (20µg)
Lane 2 : PPIF knockout HEK-293T cell lysate (20µg)
Lanes 1- 2 : Merged signal (red and green). Green - ab231155 observed at 23 kDa. Red - loading control ab8245 observed at 37 kDa.
ab231155 Anti-Cyclophilin F antibody [EPR11311-121] was shown to specifically react with Cyclophilin F in wild-type HEK-293T cells in western blot. Loss of signal was observed when knockout cell line ab266077 (knockout cell lysate ab257039) was used. Wild-type and Cyclophilin F knockout samples were subjected to SDS-PAGE. Membrane was blocked for 1 hour at room temperature in 0.1% TBST with 3% non-fat dried milk. ab231155 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated overnight at 4°C at 1 in 1000 dilution and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-Cyclophilin F antibody [EPR11311-121] (<a href='/en-us/products/primary-antibodies/cyclophilin-f-antibody-epr11311-121-ab231155'>ab231155</a>) at 1/1000 dilution
Lane 1:
Wild-type HEK-293T cell lysate at 20 µg
Lane 2:
PPIF knockout HEK-293T cell lysate at 20 µg
Lane 2:
Western blot - Human PPIF (Cyclophilin F) knockout HEK-293T cell line (<a href='/en-us/products/cell-lines/human-ppif-cyclophilin-f-knockout-hek-293t-cell-line-ab266077'>ab266077</a>)
Predicted band size: 22 kDa
Observed band size: 23 kDa
false
- Sanger seq
Unknown
Sanger Sequencing - Human PPIF (Cyclophilin F) knockout HEK-293T cell lysate (AB257039)
Homozygous : 1 bp insertion in exon 1
- WB
Lab
Western blot - Human PPIF (Cyclophilin F) knockout HEK-293T cell lysate (AB257039)
Lane 1 : Wild-type HEK-293T cell lysate (20µg)
Lane 2 : PPIF knockout HEK-293T cell lysate (20µg)
Lanes 1- 2 : Merged signal (red and green). Green - ab110324 observed at 23 kDa. Red - loading control ab181602 observed at 37 kDa.
ab110324 Anti-Cyclophilin F antibody [E11AE12BD4] was shown to specifically react with Cyclophilin F in wild-type HEK-293T cells in western blot. Loss of signal was observed when knockout cell line ab266077 (knockout cell lysate ab257039) was used. Wild-type and Cyclophilin F knockout samples were subjected to SDS-PAGE. Membrane was blocked for 1 hour at room temperature in 0.1% TBST with 3% non-fat dried milk. ab110324 and Anti-GAPDH antibody[EPR16891] - Loading Control (ab181602) were incubated overnight at 4°C at 1 in 10000 dilution and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed (ab216772) and Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed (ab216777) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-Cyclophilin F antibody [E11AE12BD4] (<a href='/en-us/products/primary-antibodies/cyclophilin-f-antibody-e11ae12bd4-ab110324'>ab110324</a>) at 1/10000 dilution
Lane 1:
Wild-type HEK-293T cell lysate at 20 µg
Lane 2:
Western blot - Human PPIF (Cyclophilin F) knockout HEK-293T cell lysate (ab257039) at 20 µg
Predicted band size: 22 kDa
Observed band size: 37 kDa,23 kDa
false
Reactivity data
Product details
Knockout cell lysate achieved by CRISPR/Cas9.
REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.
Lysate preparation: Our lysates are made using RIPA buffer to which we add a protease inhibitor cocktail and phosphatase inhibitor cocktail (ratio: 300:100:10). This means that the protein of interest is denatured. If you require a native form of the protein please use the live cell version. Please refer to our lysis protocol for further details on how our lysates are prepared.
User storage instructions: Lyophilizate may be stored at 4°C. After reconstitution, store at -20°C for short-term storage or -80°C for long-term storage.
This product is subject to limited use licenses from The Broad Institute, ERS Genomics Limited and Sigma-Aldrich Co. LLC, and is developed with patented technology. For full details of the licenses and patents please refer to our limited use license and patent pages.
What's included?
Properties and storage information
Gene name
Gene editing type
Gene editing method
Knockout validation
Zygosity
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Quality control
STR analysis
CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX
Cell culture
Biosafety level
EU: 2 US: 2
Adherent/suspension
Adherent
Gender
Female
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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