Bio-Connect

Search results: LOX CRISPR

409 to 420 of 220.715 products
Sort by
Figure 1. Western blot analysis of Olr1 using anti-Olr1 antibody (A00760-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse brain tissue lysates, Lane 2: mouse liver tissue lysates, Lane 3: mouse kidney tissue lysates, Lane 4: mouse smooth muscle tissue lysates, Lane 5: mouse SP2/0 whole cell lysates, Lane 6: mouse Neuro-2a whole cell lysates, Lane 7: rat brain tissue lysates, Lane 8: rat liver tissue lysates, Lane 9: rat kidney tissue lysates, Lane 10: rat smooth muscle tissue lysates, Lane 11: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Olr1 antigen affinity purified polyclonal antibody (Catalog # A00760-3) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Olr1 at approximately 52 kDa. The expected band size for Olr1 is at 42 kDa.
Product group Antibodies
Boster Bio
ApplicationsFlow Cytometry, Western Blot, ELISA, ImmunoHistoChemistry
ReactivityMouse, Rat
TargetOlr1
  • SizePrice
Figure 1. Western blot analysis of Olr1 using anti-Olr1 antibody (A00760-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse brain tissue lysates, Lane 2: mouse liver tissue lysates, Lane 3: mouse kidney tissue lysates, Lane 4: mouse smooth muscle tissue lysates, Lane 5: mouse SP2/0 whole cell lysates, Lane 6: mouse Neuro-2a whole cell lysates, Lane 7: rat brain tissue lysates, Lane 8: rat liver tissue lysates, Lane 9: rat kidney tissue lysates, Lane 10: rat smooth muscle tissue lysates, Lane 11: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Olr1 antigen affinity purified polyclonal antibody (Catalog # A00760-3) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Olr1 at approximately 52 kDa. The expected band size for Olr1 is at 42 kDa.
Product group Antibodies
Boster Bio
ApplicationsFlow Cytometry, Western Blot, ELISA, ImmunoHistoChemistry
ReactivityMouse, Rat
TargetOlr1
  • SizePrice
Figure 1. Western blot analysis of Olr1 using anti-Olr1 antibody (A00760-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse brain tissue lysates, Lane 2: mouse liver tissue lysates, Lane 3: mouse kidney tissue lysates, Lane 4: mouse smooth muscle tissue lysates, Lane 5: mouse SP2/0 whole cell lysates, Lane 6: mouse Neuro-2a whole cell lysates, Lane 7: rat brain tissue lysates, Lane 8: rat liver tissue lysates, Lane 9: rat kidney tissue lysates, Lane 10: rat smooth muscle tissue lysates, Lane 11: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Olr1 antigen affinity purified polyclonal antibody (Catalog # A00760-3) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Olr1 at approximately 52 kDa. The expected band size for Olr1 is at 42 kDa.
Product group Antibodies
Boster Bio
ApplicationsFlow Cytometry, Western Blot, ELISA, ImmunoHistoChemistry
ReactivityMouse, Rat
TargetOlr1
  • SizePrice
Figure 1. Western blot analysis of LOX 1/OLR1 using anti-LOX 1/OLR1 antibody (PA1832). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human prostatic carcinoma tissue (PCT) lysates, Lane 2: human cervical carcinoma tissue (CCAT) lysates, Lane 3: human gallbladder carcinoma tissue (GBCT) lysates, Lane 4: human intrahepatic cholangiocarcinom paracancerous tissue (ICCP) lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LOX 1/OLR1 antigen affinity purified polyclonal antibody (Catalog # PA1832) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 fo r 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LOX 1/OLR1 at approximately 48-52 kDa. The expected band size for LOX 1/OLR1 is at 31 kDa.
Product group Antibodies
Boster Bio
ApplicationsWestern Blot
ReactivityHuman
TargetOLR1
  • SizePrice
Figure 1. Western blot analysis of LOX 1/OLR1 using anti-LOX 1/OLR1 antibody (PA1832). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human prostatic carcinoma tissue (PCT) lysates, Lane 2: human cervical carcinoma tissue (CCAT) lysates, Lane 3: human gallbladder carcinoma tissue (GBCT) lysates, Lane 4: human intrahepatic cholangiocarcinom paracancerous tissue (ICCP) lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LOX 1/OLR1 antigen affinity purified polyclonal antibody (Catalog # PA1832) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 fo r 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LOX 1/OLR1 at approximately 48-52 kDa. The expected band size for LOX 1/OLR1 is at 31 kDa.
Product group Antibodies
Boster Bio
ApplicationsWestern Blot
ReactivityHuman
TargetOLR1
  • SizePrice
Figure 1. Western blot analysis of LOX 1/OLR1 using anti-LOX 1/OLR1 antibody (PA1832). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human prostatic carcinoma tissue (PCT) lysates, Lane 2: human cervical carcinoma tissue (CCAT) lysates, Lane 3: human gallbladder carcinoma tissue (GBCT) lysates, Lane 4: human intrahepatic cholangiocarcinom paracancerous tissue (ICCP) lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LOX 1/OLR1 antigen affinity purified polyclonal antibody (Catalog # PA1832) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 fo r 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LOX 1/OLR1 at approximately 48-52 kDa. The expected band size for LOX 1/OLR1 is at 31 kDa.
Product group Antibodies
Boster Bio
ApplicationsWestern Blot
ReactivityHuman
TargetOLR1
  • SizePrice
Figure 1. Western blot analysis of LOX 1/OLR1 using anti-LOX 1/OLR1 antibody (PA1832). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human prostatic carcinoma tissue (PCT) lysates, Lane 2: human cervical carcinoma tissue (CCAT) lysates, Lane 3: human gallbladder carcinoma tissue (GBCT) lysates, Lane 4: human intrahepatic cholangiocarcinom paracancerous tissue (ICCP) lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LOX 1/OLR1 antigen affinity purified polyclonal antibody (Catalog # PA1832) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 fo r 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LOX 1/OLR1 at approximately 48-52 kDa. The expected band size for LOX 1/OLR1 is at 31 kDa.
Product group Antibodies
Boster Bio
ApplicationsWestern Blot
ReactivityHuman
TargetOLR1
  • SizePrice
Figure 1. Western blot analysis of LOX 1/OLR1 using anti-LOX 1/OLR1 antibody (PA1832). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human prostatic carcinoma tissue (PCT) lysates, Lane 2: human cervical carcinoma tissue (CCAT) lysates, Lane 3: human gallbladder carcinoma tissue (GBCT) lysates, Lane 4: human intrahepatic cholangiocarcinom paracancerous tissue (ICCP) lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LOX 1/OLR1 antigen affinity purified polyclonal antibody (Catalog # PA1832) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 fo r 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LOX 1/OLR1 at approximately 48-52 kDa. The expected band size for LOX 1/OLR1 is at 31 kDa.
Product group Antibodies
Boster Bio
ApplicationsWestern Blot
ReactivityHuman
TargetOLR1
  • SizePrice
Figure 1. Western blot analysis of LOX 1/OLR1 using anti-LOX 1/OLR1 antibody (PA1832). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human prostatic carcinoma tissue (PCT) lysates, Lane 2: human cervical carcinoma tissue (CCAT) lysates, Lane 3: human gallbladder carcinoma tissue (GBCT) lysates, Lane 4: human intrahepatic cholangiocarcinom paracancerous tissue (ICCP) lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LOX 1/OLR1 antigen affinity purified polyclonal antibody (Catalog # PA1832) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 fo r 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LOX 1/OLR1 at approximately 48-52 kDa. The expected band size for LOX 1/OLR1 is at 31 kDa.
Product group Antibodies
Boster Bio
ApplicationsWestern Blot
ReactivityHuman
TargetOLR1
  • SizePrice
Figure 1. Western blot analysis of LOX 1/OLR1 using anti-LOX 1/OLR1 antibody (PA1832). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human prostatic carcinoma tissue (PCT) lysates, Lane 2: human cervical carcinoma tissue (CCAT) lysates, Lane 3: human gallbladder carcinoma tissue (GBCT) lysates, Lane 4: human intrahepatic cholangiocarcinom paracancerous tissue (ICCP) lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LOX 1/OLR1 antigen affinity purified polyclonal antibody (Catalog # PA1832) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 fo r 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LOX 1/OLR1 at approximately 48-52 kDa. The expected band size for LOX 1/OLR1 is at 31 kDa.
Product group Antibodies
Boster Bio
ApplicationsWestern Blot
ReactivityHuman
TargetOLR1
  • SizePrice
Figure 1. Western blot analysis of LOX 1/OLR1 using anti-LOX 1/OLR1 antibody (PA1832). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human prostatic carcinoma tissue (PCT) lysates, Lane 2: human cervical carcinoma tissue (CCAT) lysates, Lane 3: human gallbladder carcinoma tissue (GBCT) lysates, Lane 4: human intrahepatic cholangiocarcinom paracancerous tissue (ICCP) lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LOX 1/OLR1 antigen affinity purified polyclonal antibody (Catalog # PA1832) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 fo r 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LOX 1/OLR1 at approximately 48-52 kDa. The expected band size for LOX 1/OLR1 is at 31 kDa.
Product group Antibodies
Boster Bio
ApplicationsWestern Blot
ReactivityHuman
TargetOLR1
  • SizePrice
Figure 1. Western blot analysis of LOX 1/OLR1 using anti-LOX 1/OLR1 antibody (PA1832). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human prostatic carcinoma tissue (PCT) lysates, Lane 2: human cervical carcinoma tissue (CCAT) lysates, Lane 3: human gallbladder carcinoma tissue (GBCT) lysates, Lane 4: human intrahepatic cholangiocarcinom paracancerous tissue (ICCP) lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LOX 1/OLR1 antigen affinity purified polyclonal antibody (Catalog # PA1832) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 fo r 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LOX 1/OLR1 at approximately 48-52 kDa. The expected band size for LOX 1/OLR1 is at 31 kDa.
Product group Antibodies
Boster Bio
ApplicationsWestern Blot
ReactivityHuman
TargetOLR1
  • SizePrice

Didn't find what you were looking for?

Search through our product groups to find the right product

Back to overview
AntibodiesChemicalsProteins / Signaling MoleculesAssaysDNA / RNA / VectorsCell CultureGenome Editing and EngineeringMolecular BiologyLysates / ExtractsExpressionLabware / AccesoriesBody ProductsTechnique Specific ProductsArrays / SlidesDiagnosticBiologicalsMicrobiologyPromotions