Search results: Dengue virus
Product group Antibodies
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
ReactivityVirus
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Product group Antibodies
ApplicationsWestern Blot
ReactivityVirus
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Product group Antibodies
ApplicationsWestern Blot
ReactivityVirus
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Product group Antibodies
ApplicationsWestern Blot
ReactivityVirus
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Product group Antibodies
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
ReactivityVirus
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Product group Antibodies
ApplicationsImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry
ReactivityVirus
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Product group Antibodies
ApplicationsWestern Blot
ReactivityVirus
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Product group Antibodies
ApplicationsImmunoFluorescence, ImmunoCytoChemistry
ReactivityVirus
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Product group Antibodies
ApplicationsWestern Blot
ReactivityVirus
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Product group Antibodies
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
ReactivityVirus
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Product group Antibodies
ApplicationsWestern Blot, ELISA
ReactivityVirus
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Product group Antibodies
ApplicationsWestern Blot
ReactivityVirus
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Back to overview![Yellow Fever Virus viral lysate (0.1 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with Yellow Fever virus Envelope Protein antibody [HL2730] (GTX639558) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.](https://www.genetex.com/upload/website/prouct_img/normal/GTX639558/GTX639558_T-45264_20240105_WB_YFV_24010821_782.webp)
![Non-infected (–) and infected (+) H1299 whole cell extracts were separated by 7.5% SDS-PAGE, and the membrane was blotted with Influenza A virus H1N1 HA (Hemagglutinin) antibody [HL3261] (GTX640908) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.](https://www.genetex.com/upload/website/prouct_img/normal/GTX640908/GTX640908_T-45523_20240913_WB_H1N1_24091901_929.webp)


![Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with West Nile virus prM protein antibody [HL3351] (GTX641128) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.](https://www.genetex.com/upload/website/prouct_img/normal/GTX641128/GTX641128_T-45565_20241018_WB_WNV_B_24102323_353.webp)

![Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with Respiratory Syncytial virus type A G protein antibody [HL3122] (GTX640598) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](https://www.genetex.com/upload/website/prouct_img/normal/GTX640598/GTX640598_T-45460_20240809_WB_RSV_multiple_B_24081300_536.webp)
![Respiratory Syncytial virus Fusion protein antibody [GT14] detects Respiratory Syncytial virus Fusion protein by immunofluorescent analysis. Sample: Mock and transfected 293T cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: Respiratory Syncytial virus Fusion protein stained by Respiratory Syncytial virus Fusion protein antibody [GT14] (GTX640819) diluted at 1:500. Blue: Fluoroshield with DAPI (GTX30920).](https://www.genetex.com/upload/website/prouct_img/normal/GTX640819/GTX640819_45495_20240920_ICC_IF_RSV_B_24092600_596.webp)
![Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with West Nile virus prM protein antibody [HL3500] (GTX641388) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.](https://www.genetex.com/upload/website/prouct_img/normal/GTX641388/GTX641388_T-45607_20241213_WB_WNV_B_24121918_988.webp)