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Figure 1. IHC analysis of Von Willebrand Factor/VWF using anti-Von Willebrand Factor/VWF antibody (A00270-1). Von Willebrand Factor/VWF was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 microg/ml rabbit anti-Von Willebrand Factor/VWF Antibody (A00270-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
Product group Antibodies
Boster Bio
Anti-Von Willebrand Factor/VWF AntibodyA00270-1-DYLIGHT488
ApplicationsELISA, ImmunoHistoChemistry
ReactivityHuman
TargetVWF
  • SizePrice
Figure 1. IHC analysis of Von Willebrand Factor/VWF using anti-Von Willebrand Factor/VWF antibody (A00270-1). Von Willebrand Factor/VWF was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 microg/ml rabbit anti-Von Willebrand Factor/VWF Antibody (A00270-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
Product group Antibodies
Boster Bio
Anti-Von Willebrand Factor/VWF AntibodyA00270-1-DYLIGHT550
ApplicationsELISA, ImmunoHistoChemistry
ReactivityHuman
TargetVWF
  • SizePrice
Figure 1. IHC analysis of Von Willebrand Factor/VWF using anti-Von Willebrand Factor/VWF antibody (A00270-1). Von Willebrand Factor/VWF was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 microg/ml rabbit anti-Von Willebrand Factor/VWF Antibody (A00270-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
Product group Antibodies
Boster Bio
Anti-Von Willebrand Factor/VWF AntibodyA00270-1-DYLIGHT594
ApplicationsELISA, ImmunoHistoChemistry
ReactivityHuman
TargetVWF
  • SizePrice
Figure 1. IHC analysis of Von Willebrand Factor/VWF using anti-Von Willebrand Factor/VWF antibody (A00270-1). Von Willebrand Factor/VWF was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 microg/ml rabbit anti-Von Willebrand Factor/VWF Antibody (A00270-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
Product group Antibodies
Boster Bio
Anti-Von Willebrand Factor/VWF AntibodyA00270-1-FITC
ApplicationsELISA, ImmunoHistoChemistry
ReactivityHuman
TargetVWF
  • SizePrice
Figure 1. IHC analysis of Von Willebrand Factor/VWF using anti-Von Willebrand Factor/VWF antibody (A00270-1). Von Willebrand Factor/VWF was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 microg/ml rabbit anti-Von Willebrand Factor/VWF Antibody (A00270-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
Product group Antibodies
Boster Bio
Anti-Von Willebrand Factor/VWF AntibodyA00270-1-HRP
ApplicationsELISA, ImmunoHistoChemistry
ReactivityHuman
TargetVWF
  • SizePrice
Figure 1. IHC analysis of Von Willebrand Factor/VWF using anti-Von Willebrand Factor/VWF antibody (A00270-1). Von Willebrand Factor/VWF was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 microg/ml rabbit anti-Von Willebrand Factor/VWF Antibody (A00270-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
Product group Antibodies
Boster Bio
Anti-Von Willebrand Factor/VWF AntibodyA00270-1-IFLUOR647
ApplicationsELISA, ImmunoHistoChemistry
ReactivityHuman
TargetVWF
  • SizePrice
Figure 1. IHC analysis of Von Willebrand Factor/VWF using anti-Von Willebrand Factor/VWF antibody (A00270-1). Von Willebrand Factor/VWF was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 microg/ml rabbit anti-Von Willebrand Factor/VWF Antibody (A00270-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
Product group Antibodies
Boster Bio
Anti-Von Willebrand Factor/VWF AntibodyA00270-1-PE
ApplicationsELISA, ImmunoHistoChemistry
ReactivityHuman
TargetVWF
  • SizePrice
Figure 1. IHC analysis of Von Willebrand Factor/VWF using anti-Von Willebrand Factor/VWF antibody (A00270-1). Von Willebrand Factor/VWF was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 microg/ml rabbit anti-Von Willebrand Factor/VWF Antibody (A00270-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
Product group Antibodies
References
Boster Bio
Anti-Von Willebrand Factor/VWF AntibodyA00270-1
ApplicationsELISA, ImmunoHistoChemistry
ReactivityHuman
TargetVWF
  • SizePrice
Figure 1. Immunohistochemistry validation of VWF using Anti-von Willebrand factor VWF Antibody (A00270). Immunohistochemistry (IHC) analyzes of VWF pAb in paraffin-embedded human colon carcinoma tissue at 1:50
Product group Antibodies
Boster Bio
Anti-von Willebrand factor VWF AntibodyA00270
ApplicationsImmunoHistoChemistry
ReactivityHuman, Mouse, Rat
TargetVWF
  • SizePrice
Figure 1. Western blot analysis of HEBP1 using anti-HEBP1 antibody (A00271-1). 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 A549 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human hepatocellular carcinoma tumor tissue (HCCT) lysates, Lane 4: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue 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-HEBP1 antigen affinity purified polyclonal antibody (Catalog # A00271-1) 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 HEBP1 at approximately 21 kDa. The expected band size for HEBP1 is at 21 kDa.
Product group Antibodies
Boster Bio
Anti-HEBP1 Antibody Picoband(r)A00271-1-BIOTIN
ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry
ReactivityHuman, Mouse, Rat
TargetHEBP1
  • SizePrice
Figure 1. Western blot analysis of HEBP1 using anti-HEBP1 antibody (A00271-1). 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 A549 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human hepatocellular carcinoma tumor tissue (HCCT) lysates, Lane 4: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue 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-HEBP1 antigen affinity purified polyclonal antibody (Catalog # A00271-1) 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 HEBP1 at approximately 21 kDa. The expected band size for HEBP1 is at 21 kDa.
Product group Antibodies
Boster Bio
Anti-HEBP1 Antibody Picoband(r)A00271-1-CARRIER-FREE
ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry
ReactivityHuman, Mouse, Rat
TargetHEBP1
  • SizePrice
Figure 1. Western blot analysis of HEBP1 using anti-HEBP1 antibody (A00271-1). 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 A549 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human hepatocellular carcinoma tumor tissue (HCCT) lysates, Lane 4: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue 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-HEBP1 antigen affinity purified polyclonal antibody (Catalog # A00271-1) 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 HEBP1 at approximately 21 kDa. The expected band size for HEBP1 is at 21 kDa.
Product group Antibodies
Boster Bio
Anti-HEBP1 Antibody Picoband(r)A00271-1-CY3
ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry
ReactivityHuman, Mouse, Rat
TargetHEBP1
  • SizePrice
23456

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