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ProductsBack/Human Plasma EDTA K3 Mixed Gender Pooled, Ultrafiltrate

Human Plasma EDTA K3 Mixed Gender Pooled, Ultrafiltrate

Research Use Only
HMPLEDTA3-ULTRA-P-M
BioIVT
Product group Body Products
Price on request
500 ml
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More than 130 suppliers
ISO certified
In-house tech support

Overview

  • Supplier
    BioIVT
  • Product Name
    Human Plasma EDTA K3 Mixed Gender Pooled, Ultrafiltrate
  • Delivery Days Customer
    9
  • Certification
    Research Use Only
  • UNSPSC
    41105901

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Figure 1. Western blot analysis of RUFY1 using anti-RUFY1 antibody (A10201-1). 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 Hela whole cell lysates, Lane 2: human SiHa 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-RUFY1 antigen affinity purified polyclonal antibody (Catalog # A10201-1) 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 RUFY1 at approximately 80 kDa. The expected band size for RUFY1 is at 80 kDa.
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Figure 1. Western blot analysis of QSOX2 using anti-QSOX2 antibody (A10205-1). 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 Hela whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human A549 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-QSOX2 antigen affinity purified polyclonal antibody (Catalog # A10205-1) at 0.25 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 QSOX2 at approximately 80 kDa. The expected band size for QSOX2 is at 80 kDa.
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Figure 1. Western blot analysis of QSOX2 using anti-QSOX2 antibody (A10205-1). 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 Hela whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human A549 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-QSOX2 antigen affinity purified polyclonal antibody (Catalog # A10205-1) at 0.25 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 QSOX2 at approximately 80 kDa. The expected band size for QSOX2 is at 80 kDa.
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