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![Immunohistochemistry-Paraffin: Normal Rabbit Serum [NBP1-71681] - Frozen newborn mouse cartilage sections were blocked with (SB Cat. No. 0040-01) and stained with Mouse Anti-Collagen Type II-UNLB (right) followed by Rabbit F(ab')2 Anti-Mouse IgG(H+L), Human ads-BIOT (SB Cat. No. 6125-08), Streptavidin-CY3.5 (SB Cat. No. 7100-24), DAPI, and mounted with Fluoromount-G Anti-Fade (SB Cat. No. 0100-35).](http://images.novusbio.com/fullsize/Normal-Rabbit-Serum-Immunohistochemistry-Paraffin-NBP1-71681-img0004.jpg "Immunohistochemistry-Paraffin: Normal Rabbit Serum [NBP1-71681] - Frozen newborn mouse cartilage sections were blocked with (SB Cat. No. 0040-01) and stained with Mouse Anti-Collagen Type II-UNLB (right) followed by Rabbit F(ab')2 Anti-Mouse IgG(H+L), Human ads-BIOT (SB Cat. No. 6125-08), Streptavidin-CY3.5 (SB Cat. No. 7100-24), DAPI, and mounted with Fluoromount-G Anti-Fade (SB Cat. No. 0100-35).")
![Immunohistochemistry-Paraffin: Normal Rabbit Serum [NBP1-71681] - Paraffin embedded mouse small intestine tissue section was blocked with (SB Cat. No. 0040-01) and stained with Goat Anti-Mouse IgA-UNLB (SB Cat. No. 1040-01) followed by Rabbit Anti-Goat IgG(H+L), Human SP ads-BIOT (SB Cat. No. 6164-08), Streptavidin-CY3 (SB Cat. No. 7100-12), DAPI, and mounted with Fluoromount-G® Anti-Fade (SB Cat. No. 0100-35).](http://images.novusbio.com/fullsize/Normal-Rabbit-Serum-Immunohistochemistry-Paraffin-NBP1-71681-img0002.jpg)
![Immunohistochemistry-Paraffin: Normal Rabbit Serum [NBP1-71681] - Paraffin embedded mouse small intestine tissue section was blocked with (SB Cat. No. 0040-01) and stained with Rat Anti-Mouse IgA-UNLB (SB Cat. No. 1165-01) followed by Rabbit Anti-Rat IgG(H+L), Human ads-BIOT (SB Cat. No. 6185-08), Streptavidin-FITC (SB Cat. No. 7100-02), DAPI, and mounted with Fluoromount-G® Anti-Fade (SB Cat. No. 0100-35).](http://images.novusbio.com/fullsize/Normal-Rabbit-Serum-Immunohistochemistry-Paraffin-NBP1-71681-img0003.jpg)
![Fluorescence Imaging: Normal Rabbit Serum [NBP1-71681] - Frozen newborn mouse cartilage sections were blocked with (SB Cat. No. 0040-01) and stained with Mouse Anti-Collagen Type II-UNLB (right) followed by Rabbit F(ab')2 Anti-Mouse IgG(H+L), Human ads-BIOT (SB Cat. No. 6125-08), Streptavidin-FITC (SB Cat. No. 7100-02), DAPI, and mounted with Fluoromount-G® Anti-Fade (SB Cat. No. 0100-35).](http://images.novusbio.com/fullsize/Normal-Rabbit-Serum-Fluorescence-Imaging-NBP1-71681-img0001.jpg)
![Zymosan, TLR2 Ligand [NBP2-26233] - Ligand activity of Zymosan. The NF-kB/SEAPorter/HEK 293 and TLR2/NFkB/SEAPorter/ HEK 293 cell line cell lines were plated in a 96-well plate at 5 x 10^4 cells/well for 16 h. Cells were then stimulated with Zymosan for 24h. The cell culture supernatants were analyzed for SEAP activity using SEAPorter Assay Kit.](http://images.novusbio.com/fullsize/Zymosan--TLR2-Ligand-NBP2-26233-img0002.jpg "Zymosan, TLR2 Ligand [NBP2-26233] - Ligand activity of Zymosan. The NF-kB/SEAPorter/HEK 293 and TLR2/NFkB/SEAPorter/ HEK 293 cell line cell lines were plated in a 96-well plate at 5 x 10^4 cells/well for 16 h. Cells were then stimulated with Zymosan for 24h. The cell culture supernatants were analyzed for SEAP activity using SEAPorter Assay Kit.")
![Immunohistochemistry: VECTASHIELD(R) Antifade Mounting Medium [H-1000-NB] - Multiple labeling of colon with Fluorescein (green), Texas Red(R) (red), and AMCA (blue) mounted with VECTASHIELD Mounting Medium.](http://images.novusbio.com/fullsize/VECTASHIELD-R-Antifade-Mounting-Medium-Immunohistochemistry-H-1000-NB-img0027.jpg "Immunohistochemistry: VECTASHIELD(R) Antifade Mounting Medium [H-1000-NB] - Multiple labeling of colon with Fluorescein (green), Texas Red(R) (red), and AMCA (blue) mounted with VECTASHIELD Mounting Medium.")
![Immunohistochemistry: VECTASHIELD(R) Antifade Mounting Medium [H-1000-NB] - Colon stained with fluorescein labeled Amaranthus caudatus lectin mounted with VECTASHIELD Mounting Medium.](http://images.novusbio.com/fullsize/VECTASHIELD-R-Antifade-Mounting-Medium-Immunohistochemistry-H-1000-NB-img0026.jpg)
![Immunofluorescence: VECTASHIELD(R) Antifade Mounting Medium [H-1000-NB] - STORM imaging of Alexa Fluor 647 stained microtubules in VECTASHIELD Mounting Medium. (Image kindly supplied by Dr. Nicolas Olivier, King's College, London UK.)](http://images.novusbio.com/fullsize/VECTASHIELD-R-Antifade-Mounting-Medium-Immunofluorescence-H-1000-NB-img0021.jpg)
![Immunofluorescence: VECTASHIELD(R) Antifade Mounting Medium [H-1000-NB] - STORM imaging of Alexa Fluor 647 stained microtubules in VECTASHIELD Mounting Medium. (Image kindly supplied by Dr. Nicolas Olivier, King's College, London UK.)](http://images.novusbio.com/fullsize/VECTASHIELD-R-Antifade-Mounting-Medium-Immunofluorescence-H-1000-NB-img0022.jpg)
![Immunofluorescence: VECTASHIELD(R) Antifade Mounting Medium [H-1000-NB] - STORM imaging of Alexa Fluor 647 stained microtubules in VECTASHIELD Mounting Medium. (Image kindly supplied by Dr. Nicolas Olivier, King's College, London UK.)](http://images.novusbio.com/fullsize/VECTASHIELD-R-Antifade-Mounting-Medium-Immunofluorescence-H-1000-NB-img0023.jpg)
![Immunofluorescence: VECTASHIELD(R) Antifade Mounting Medium [H-1000-NB] - STORM imaging of Alexa Fluor 647 stained microtubules in VECTASHIELD Mounting Medium. (Image kindly supplied by Dr. Nicolas Olivier, King's College, London UK.)](http://images.novusbio.com/fullsize/VECTASHIELD-R-Antifade-Mounting-Medium-Immunofluorescence-H-1000-NB-img0024.jpg)
![Immunofluorescence: VECTASHIELD(R) Antifade Mounting Medium [H-1000-NB] - STORM imaging of Alexa Fluor 647 stained microtubules in VECTASHIELD Mounting Medium. (Image kindly supplied by Dr. Nicolas Olivier, King's College, London UK.)](http://images.novusbio.com/fullsize/VECTASHIELD-R-Antifade-Mounting-Medium-Immunofluorescence-H-1000-NB-img0025.jpg)
![Immunofluorescence: VECTASHIELD(R) Antifade Mounting Medium [H-1000-NB] - 3D STORM imaging of Alexa Fluor 647 stained microtubules in a VECTASHIELD Mounting Medium/TRIS-Glycerol mixture. (Image kindly supplied by Dr. Nicolas Olivier, King's College, London UK.)](http://images.novusbio.com/fullsize/VECTASHIELD-R-Antifade-Mounting-Medium-Immunofluorescence-H-1000-NB-img0028.jpg)
![Immunofluorescence: VECTASHIELD(R) Antifade Mounting Medium [H-1000-NB] - 3D STORM imaging of Alexa Fluor 647 stained microtubules in a VECTASHIELD Mounting Medium/TRIS-Glycerol mixture. (Image kindly supplied by Dr. Nicolas Olivier, King's College, London UK.)](http://images.novusbio.com/fullsize/VECTASHIELD-R-Antifade-Mounting-Medium-Immunofluorescence-H-1000-NB-img0029.jpg)
![Immunocytochemistry/Immunofluorescence: Dicer knockout Mouse embryonic stem cells [NBP1-96751] - SSEA1 antibody (NB100-1831) was tested in Dicer knockout Mouse embryonic stem cells with DyLight 488 (green). Nuclei were counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/Dicer-knockout-Mouse-embryonic-stem-cells-Immunocytochemistry-Immunofluorescence-NBP1-96751-img0003.jpg "<b>Genetic Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: Dicer knockout Mouse embryonic stem cells [NBP1-96751] - SSEA1 antibody (NB100-1831) was tested in Dicer knockout Mouse embryonic stem cells with DyLight 488 (green). Nuclei were counterstained with DAPI (blue).")
![<b>Genetic Strategies Validation. </b>Immunohistochemistry: Dicer knockout Mouse embryonic stem cells [NBP1-96751] - Brightfield Image of Dicer knock out Mouse embryonic stem cell line colonies growing directly on a gelatinized tissue culture flask.](http://images.novusbio.com/fullsize/Dicer-knockout-Mouse-embryonic-stem-cells-Immunohistochemistry-NBP1-96751-img0004.jpg)
![<b>Genetic Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: Dicer knockout Mouse embryonic stem cells [NBP1-96751] - Nanog antibody (NB100-58842) was tested in Dicer knockout Mouse embryonic stem cells with DyLight 488 (green). Nuclei were counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/Dicer-knockout-Mouse-embryonic-stem-cells-Immunocytochemistry-Immunofluorescence-NBP1-96751-img0002.jpg)
![Live Imaging Microscopy: DRAQ5 (TM) [NBP2-81125] - DRAQ5 was diluted in EMEM culture media and applied to live HeLa cells at 5 uM (1:1000) for 30 minutes at room temperature and protected from light. Imaging was done immediately after staining without washing the cells.](http://images.novusbio.com/fullsize/DRAQ5-TM-Live-Imaging-Microscopy-NBP2-81125-img0007.jpg "Live Imaging Microscopy: DRAQ5 (TM) [NBP2-81125] - DRAQ5 was diluted in EMEM culture media and applied to live HeLa cells at 5 uM (1:1000) for 30 minutes at room temperature and protected from light. Imaging was done immediately after staining without washing the cells.")
![Immunocytochemistry/Immunofluorescence: DRAQ5 (TM) [NBP2-81125] - ' (red) counterstaining of fixed U2OS cells. AlexaFluor 488 antibody to beta-tubulin (green).](http://images.novusbio.com/fullsize/DRAQ5-TM-Immunocytochemistry-Immunofluorescence-NBP2-81125-img0003.jpg)
![Flow Cytometry: DRAQ5 (TM) [NBP2-81125] - DNA content analysis in live or fixed cells using DRAQ5 (TM)](http://images.novusbio.com/fullsize/DRAQ5-TM-Flow-Cytometry-NBP2-81125-img0006.jpg)
![Immunocytochemistry/Immunofluorescence: DRAQ5 (TM) [NBP2-81125] - used to stain dsDNA of dividing cells.](http://images.novusbio.com/fullsize/DRAQ5-TM-Immunocytochemistry-Immunofluorescence-NBP2-81125-img0004.jpg)
![Flow Cytometry: DRAQ5 (TM) [NBP2-81125] - No lyse, no wash gating of nucleated cells from whole bone marrow gating on DRAQ5 (TM) signal.](http://images.novusbio.com/fullsize/DRAQ5-TM-Flow-Cytometry-NBP2-81125-img0005.jpg)
![DRAQ5 (TM) [NBP2-81125] - Excitation and Emission Spectra for DRAQ5 (TM).](http://images.novusbio.com/fullsize/DRAQ5-TM-NBP2-81125-img0001.jpg)
![CpG oligodeoxynucleotides with negative control, TLR9 ligand [NBP2-26232] - Validation of CpG using the TLR9/HEK 293 cell line. The assay was performed using the NF-kB SEAPorter Assay Kit. The Vector/HEK 293 and TLR9/HEK 293 cell lines were transfected with NF-kB/SEAP reporter plasmid for 16 h. Cells were stimulated with various amounts of CpG for 24 h followed by SEAP assay.](http://images.novusbio.com/fullsize/CpG-oligodeoxynucleotides-with-negative-control--TLR9-ligand-NBP2-26232-img0002.jpg "CpG oligodeoxynucleotides with negative control, TLR9 ligand [NBP2-26232] - Validation of CpG using the TLR9/HEK 293 cell line. The assay was performed using the NF-kB SEAPorter Assay Kit. The Vector/HEK 293 and TLR9/HEK 293 cell lines were transfected with NF-kB/SEAP reporter plasmid for 16 h. Cells were stimulated with various amounts of CpG for 24 h followed by SEAP assay.")
![Immunocytochemistry/Immunofluorescence: DGCR8 knockout MEF cells [NBP2-25171] - The DGCR8 knockout MEF cells were stained for alpha Tubulin at a 1:1000 dilution against Dylight 550 (Red) to show composition of cell structure. Nuclei were counterstained with DAPI (blue)](http://images.novusbio.com/fullsize/DGCR8-knockout-MEF-cells-Immunocytochemistry-Immunofluorescence-NBP2-25171-img0003.jpg "Immunocytochemistry/Immunofluorescence: DGCR8 knockout MEF cells [NBP2-25171] - The DGCR8 knockout MEF cells were stained for alpha Tubulin at a 1:1000 dilution against Dylight 550 (Red) to show composition of cell structure. Nuclei were counterstained with DAPI (blue)")
![In vitro assay: DGCR8 knockout MEF cells [NBP2-25171] - Brightfield Image of DGCR8 MEF knockout cells](http://images.novusbio.com/fullsize/DGCR8-knockout-MEF-cells-In-vitro-assay-NBP2-25171-img0002.jpg)
![pCLNCX Retrovirus Expression Vector [NBP2-29502] - Schematic presentation of pCLNCX vector: CMV immediate early promoter/enhancer allows highefficiency transcription in 293 cells. However, this is lost during viral replication. Hence, the gene of interest cloned into Eco RI cloning site is driven by Moloney MLV and murine sarcoma virus LTR (RU5). For expression under the control of CMV early promoter/enhancer, the gene of interest should be cloned into Hind III or Cla I site.](http://images.novusbio.com/fullsize/pCLNCX-Retrovirus-Expression-Vector-NBP2-29502-img0001.jpg "pCLNCX Retrovirus Expression Vector [NBP2-29502] - Schematic presentation of pCLNCX vector: CMV immediate early promoter/enhancer allows highefficiency transcription in 293 cells. However, this is lost during viral replication. Hence, the gene of interest cloned into Eco RI cloning site is driven by Moloney MLV and murine sarcoma virus LTR (RU5). For expression under the control of CMV early promoter/enhancer, the gene of interest should be cloned into Hind III or Cla I site.")
![Red Blood Cell (RBC) Lysis Buffer [NBP2-29442] - data shows before (left) and after (right) human whole blood cells were lysed using the Red Blood Cell (RBC) lysis buffer. Image from verified customer review.](http://images.novusbio.com/fullsize/Red-Blood-Cell-RBC-Lysis-Buffer-NBP2-29442-img0002.jpg "Red Blood Cell (RBC) Lysis Buffer [NBP2-29442] - data shows before (left) and after (right) human whole blood cells were lysed using the Red Blood Cell (RBC) lysis buffer. Image from verified customer review.")
![Imidazoquinoline Resiquimod (R-848), TLR7 and TLR8 ligand [NBP2-26231] - TLR8 stimulation with R-848 measured by SEAP Expression 293T cells were transfected with pCMV/TLR8 plasmid and pNF-kB/SEAP plasmid using Lipofectamin 2000. After 48 hrs of transfection, 2 ug/mL or 5 ug/mL of R-848 was added. Cells were incubated at 37C for 24 hrs. Transfected cell supernatant was collected and analyzed using NF-kB SEAPorterAssay kit.](http://images.novusbio.com/fullsize/Imidazoquinoline-Resiquimod-R-848-TLR7-and-TLR8-ligand-NBP2-26231-img0004.jpg "Imidazoquinoline Resiquimod (R-848), TLR7 and TLR8 ligand [NBP2-26231] - TLR8 stimulation with R-848 measured by SEAP Expression 293T cells were transfected with pCMV/TLR8 plasmid and pNF-kB/SEAP plasmid using Lipofectamin 2000. After 48 hrs of transfection, 2 ug/mL or 5 ug/mL of R-848 was added. Cells were incubated at 37C for 24 hrs. Transfected cell supernatant was collected and analyzed using NF-kB SEAPorterAssay kit.")
![Imidazoquinoline Resiquimod (R-848), TLR7 and TLR8 ligand [NBP2-26231] - R-848 specifically activated the TLR7- or TLR8-depedent NF-kB/SEAP reporter cells in a dose dependent manner.](http://images.novusbio.com/fullsize/Imidazoquinoline-Resiquimod-R-848-TLR7-and-TLR8-ligand-NBP2-26231-img0005.jpg)
![Imidazoquinoline Resiquimod (R-848), TLR7 and TLR8 ligand [NBP2-26231] - Formula: C17H22N4O2](http://images.novusbio.com/fullsize/Imidazoquinoline-Resiquimod-R-848-TLR7-and-TLR8-ligand-NBP2-26231-img0007.jpg)