| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-18543-100ul | |||
| BSA Free | NBP3-18543-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-42385 | |||
| BSA Free | NBP2-42385-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-21163-100ul | |||
| BSA Free | NBP3-21163-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-05537-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-05533-50ul | |||
![Western Blot: GAPDH Antibody (RM114) [NBP2-77402] - Western blot of A431 cells, using NBP2-77402, showed a band of GAPDH at the predicted MW (~36 kDa).](http://images.novusbio.com/fullsize/GAPDH-Antibody-RM114-Western-Blot-NBP2-77402-img0002.jpg "Western Blot: GAPDH Antibody (RM114) [NBP2-77402] - Western blot of A431 cells, using NBP2-77402, showed a band of GAPDH at the predicted MW (~36 kDa).")
![Immunocytochemistry/Immunofluorescence: GAPDH Antibody (RM114) [NBP2-77402] - Immunocytochemical staining of HeLa cells, using NBP2-77402 (red). Nuclei have been labeled with DAPI (blue).](http://images.novusbio.com/fullsize/nbp2-77402_rabbit-monoclonal-gapdh-antibody-rm114-immunocytochemistry-immunofluorescence-199202502434.png)
![Western Blot: Raf-1 Antibody (1H4) [H00005894-M03] - Analysis of RAF1 expression in transfected 293T cell line by RAF1 monoclonal antibody (M03), clone 1H4. Lane 1: RAF1 transfected lysatE (73.1 KDa). Lane 2: Non-transfected lysate.](http://images.novusbio.com/fullsize/Raf-1-Antibody-1H4-Western-Blot-H00005894-M03-img0007.jpg "Western Blot: Raf-1 Antibody (1H4) [H00005894-M03] - Analysis of RAF1 expression in transfected 293T cell line by RAF1 monoclonal antibody (M03), clone 1H4. Lane 1: RAF1 transfected lysatE (73.1 KDa). Lane 2: Non-transfected lysate.")
![Western Blot: Raf-1 Antibody (1H4) [H00005894-M03] - Western blot analysis of RAF1 over-expressed 293 cell line, cotransfected with RAF1 Validated Chimera RNAi or non-transfected control. Blot probed with H00005894-M03. GAPDH (36.1 kDa) used as loading control.](http://images.novusbio.com/fullsize/Raf-1-Antibody-1H4-Western-Blot-H00005894-M03-img0002.jpg)
![Western Blot: Raf-1 Antibody (1H4) [H00005894-M03] - Analysis of RAF1 expression in HeLa.](http://images.novusbio.com/fullsize/Raf-1-Antibody-1H4-Western-Blot-H00005894-M03-img0005.jpg)
![Western Blot: Raf-1 Antibody (1H4) [H00005894-M03] - Analysis of RAF1 expression in rat brain.](http://images.novusbio.com/fullsize/Raf-1-Antibody-1H4-Western-Blot-H00005894-M03-img0006.jpg)
![Proximity Ligation Assay: Raf-1 Antibody (1H4) [H00005894-M03] - Analysis of protein-protein interactions between BAD and RAF1. HeLa cells were stained with anti-BAD rabbit purified polyclonal 1:1200 and anti-RAF1 mouse monoclonal antibody 1:50. Each red dot represents the detection of protein-protein interaction compl](http://images.novusbio.com/fullsize/Raf-1-Antibody-1H4-Proximity-Ligation-Assay-H00005894-M03-img0003.jpg)
![Proximity Ligation Assay: Raf-1 Antibody (1H4) [H00005894-M03] - Analysis of protein-protein interactions between PDGFRB and RAF1. Huh7 cells were stained with anti-PDGFRB rabbit purified polyclonal 1:600 and anti-RAF1 mouse monoclonal antibody 1:100. Each red dot represents the detection of protein-protein interaction](http://images.novusbio.com/fullsize/Raf-1-Antibody-1H4-Proximity-Ligation-Assay-H00005894-M03-img0004.jpg)
![Immunocytochemistry: Olig2 Antibody (3C9) [H00010215-M03] - Imaging of Optic Nerve: Red-H00010215-M03(Olig2), Blue-DAPI. This image was submitted via customer Review.](http://images.novusbio.com/fullsize/Olig2-Antibody-3C9-Immunocytochemistry-H00010215-M03-img0006.jpg "Immunocytochemistry: Olig2 Antibody (3C9) [H00010215-M03] - Imaging of Optic Nerve: Red-H00010215-M03(Olig2), Blue-DAPI. This image was submitted via customer Review.")
![Immunohistochemistry-Paraffin: Olig2 Antibody (3C9) [H00010215-M03] - Analysis of monoclonal antibody to OLIG2 on formalin-fixed paraffin-embedded human placenta. Antibody concentration 3 ug/ml](http://images.novusbio.com/fullsize/Olig2-Antibody-3C9-Immunohistochemistry-Paraffin-H00010215-M03-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: Olig2 Antibody (3C9) [H00010215-M03] - Analysis of monoclonal antibody to OLIG2 on HeLa cell. Antibody concentration 10 ug/ml](http://images.novusbio.com/fullsize/Olig2-Antibody-3C9-Immunocytochemistry-Immunofluorescence-H00010215-M03-img0004.jpg)
![Immunoprecipitation:ASCL1/Mash1 Antibody [NBP3-14738] - Whole cell lysate (1.0 mgper IP reaction; 20% of IP loaded) from SHP-77 cellsprepared using NETN lysis buffer. Antibodies: Rabbit antiASCL1/MASH1 recombinant monoclonal antibody used for IP at 6 ul per reaction.ASCL1/MASH1 was also immunoprecipitated by a secondantibody against a different epitope of ASCL1/MASH1 For blotting immunoprecipitatedASCL1/MASH1, was used at 1:1000.Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/ASCL1-Mash1-Antibody-NBP3-14738-img0001.jpg "Immunoprecipitation:ASCL1/Mash1 Antibody [NBP3-14738] - Whole cell lysate (1.0 mgper IP reaction; 20% of IP loaded) from SHP-77 cellsprepared using NETN lysis buffer. Antibodies: Rabbit antiASCL1/MASH1 recombinant monoclonal antibody used for IP at 6 ul per reaction.ASCL1/MASH1 was also immunoprecipitated by a secondantibody against a different epitope of ASCL1/MASH1 For blotting immunoprecipitatedASCL1/MASH1, was used at 1:1000.Chemiluminescence with an exposure time of 30 seconds.")
![Immunohistochemistry-Paraffin:ASCL1/Mash1 Antibody [NBP3-14738] -ASCL1/MASH1 recombinant monoclonal antibody [BLR164J]. Secondary: HRP-conjugated goat antirabbit IgG (A120-501P). Substrate: DAB.](http://images.novusbio.com/fullsize/nbp3-14738_rabbit-ascl1-mash1-mab-immunohistochemistry-paraffin-26720247516..jpg)
![Western Blot: ASCL1/Mash1 Antibody [NBP3-14738] - Whole cell lysate (50 ug) from HEK293T, HeLa, SHP-77, Hep-G2, and MCF-7 cells prepared using NETN lysis buffer. Antibody: Rabbit anti-ASCL1/MASH1 recombinant monoclonal antibody [BLR164J] used at 1:1000. Secondary: HRP-conjugated goat antirabbit IgG. Chemiluminescence with an exposure time of 10 seconds. Lower Panel: Rabbit antiActin recombinant monoclonal antibody [BLR057F].](http://images.novusbio.com/fullsize/nbp3-14738_rabbit-ascl1-mash1-mab-western-blot-267202475335..jpg)
![Various tissue extracts (50 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with MC1 Receptor antibody [HL1470] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-48655_rabbit-melanocortin-1-r-mc1r-mab-hl1470-western-blot-2592025864.png "Various tissue extracts (50 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with MC1 Receptor antibody [HL1470] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![<b>Independent Antibodies Validation. </b>Whole cell extract (30 ug) was separated by 12% SDS-PAGE, and the membranes were blotted with Melanocortin-1 R/MC1R antibody [HL1470] (NBP3-48655) diluted at 1:50000 and competitor's antibody diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.*The competitor is not affiliated with and does not endorse this product.](http://images.novusbio.com/fullsize/nbp3-48655_rabbit-melanocortin-1-r-mc1r-mab-hl1470-western-blot-141120251831322.jpg)
![<b>Orthogonal Strategies Validation. </b>Various whole cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with Melanocortin-1 R/MC1R antibody [HL1470] (NBP3-48655) diluted at 1:100000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.](http://images.novusbio.com/fullsize/nbp3-48655_rabbit-melanocortin-1-r-mc1r-mab-hl1470-western-blot-141120251828111.jpg)
![<b>Independent Antibodies Validation. </b>Various tissue extracts (50 ug) was separated by 12% SDS-PAGE, and the membranes were blotted with Melanocortin-1 R/MC1R antibody [HL1470] (NBP3-48655) diluted at 1:1000 and competitor's antibody (Competitor) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.*The competitor is not affiliated with and does not endorse this product.](http://images.novusbio.com/fullsize/nbp3-48655_rabbit-melanocortin-1-r-mc1r-mab-hl1470-western-blot-141120251831212.jpg)
![<b>Independent Antibodies Validation and Genetic Strategies Validation.</b>Non-transfected (-) and transfected (+) unboiled A375 whole cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membranes were blotted with Melanocortin-1 R/MC1R antibody [HL1470] (NBP3-48655) diluted at 1:5000 and competitor's antibody (Highly Cited Competitor) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.*The competitor is not affiliated withand does not endorse this product.](http://images.novusbio.com/fullsize/nbp3-48655_rabbit-melanocortin-1-r-mc1r-mab-hl1470-western-blot-141120251836367.jpg)
![Western Blot: QKI/Quaking Antibody (GT2612) [NBP3-13576] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with QKI/Quaking antibody [GT2612] (NBP3-13576) diluted at 1:5000. The HRP-conjugated anti-mouset IgG antibody (NBP2-19382) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/QKI-Quaking-Antibody-GT2612-Western-Blot-NBP3-13576-img0003.jpg "<b>Genetic Strategies Validation. </b>Western Blot: QKI/Quaking Antibody (GT2612) [NBP3-13576] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with QKI/Quaking antibody [GT2612] (NBP3-13576) diluted at 1:5000. The HRP-conjugated anti-mouset IgG antibody (NBP2-19382) was used to detect the primary antibody.")
![<b>Genetic Strategies Validation. </b>Immunohistochemistry-Paraffin: QKI/Quaking Antibody (GT2612) [NBP3-13576] - QKI/Quaking antibody [GT2612] detects QKI/Quaking protein at cytoplasm and nucleus in rat brain by immunohistochemical analysis. Sample: Paraffin-embedded rat brain. QKI/Quaking antibody [GT2612] (NBP3-13576) diluted at 1:200. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/QKI-Quaking-Antibody-GT2612-Immunohistochemistry-Paraffin-NBP3-13576-img0002.jpg)
![Immunohistochemistry-Paraffin: QKI/Quaking Antibody (GT2612) [NBP3-13576] - QKI/Quaking antibody [GT2612] detects QKI/Quaking protein at cytoplasm and nucleus in mouse brain by immunohistochemical analysis. Sample: Paraffin-embedded mouse brain. QKI/Quaking antibody [GT2612] (NBP3-13576) diluted at 1:200. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/QKI-Quaking-Antibody-GT2612-Immunohistochemistry-Paraffin-NBP3-13576-img0001.jpg)
![Immunohistochemistry-Paraffin: QKI/Quaking Antibody (GT2612) [NBP3-13576] - QKI/Quaking antibody [GT2612] detects QKI/Quaking protein at nucleus by immunohistochemical analysis.Sample: Paraffin-embedded rat brain.QKI/Quaking stained by QKI/Quaking antibody [GT2612] (NBP3-13576) diluted at 1:200.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13576_mouse-qki-quaking-mab-gt2612-91020242063387.jpg)
![Western Blot: QKI/Quaking Antibody (GT2612) [NBP3-13576] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with QKI/Quaking antibody [GT2612] (NBP3-13576) diluted at 1:1000. The HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-13576_mouse-qki-quaking-mab-gt2612-91020242021990.jpg)
![Immunohistochemistry-Paraffin: QKI/Quaking Antibody (GT2612) [NBP3-13576] - QKI/Quaking antibody [GT2612] detects QKI/Quaking protein at nucleus by immunohistochemical analysis.Sample: Paraffin-embedded mouse brain.QKI/Quaking stained by QKI/Quaking antibody [GT2612] (NBP3-13576) diluted at 1:200.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13576_mouse-qki-quaking-mab-gt2612-91020242091486.jpg)
![Western Blot: Ki67/MKI67 Antibody [NBP3-05537] - Western blot analysis of equal amounts of cell lysates using Ki67/MKI67 Antibody at a dilution of 1:10,000, (green): [1] protein standard (red), [2] rapidly growing HeLa cell cultures, [3] rapidly growing HEK293 cell cultures. Strong double bands larger than the 250kDa standard correspond to full length 345kDa and 395kDa Ki67/MKI67 isoforms, while smaller proteolytic fragments of these isoforms are also invariably detected on the blot.](http://images.novusbio.com/fullsize/Ki67-MKI67-Antibody-Western-Blot-NBP3-05537-img0002.jpg "Western Blot: Ki67/MKI67 Antibody [NBP3-05537] - Western blot analysis of equal amounts of cell lysates using Ki67/MKI67 Antibody at a dilution of 1:10,000, (green): [1] protein standard (red), [2] rapidly growing HeLa cell cultures, [3] rapidly growing HEK293 cell cultures. Strong double bands larger than the 250kDa standard correspond to full length 345kDa and 395kDa Ki67/MKI67 isoforms, while smaller proteolytic fragments of these isoforms are also invariably detected on the blot.")
![Immunocytochemistry/Immunofluorescence: Ki67/MKI67 Antibody [NBP3-05537] - Immunofluorescent analysis of HeLa cells stained with Ki67/MKI67 Antibody at a dilution of 1:5,000 in red, and mouse monoclonal antibody to fibrillarin at a dilution of 1:2,000, in green. The blue is DAPI staining of nuclear DNA. The Ki67/MKI67 protein accumulates in and around the nucleoli of interphase cells such as those on the right, and the nucleoli are revealed by the fibrillarin antibody. In contrast, cells in the quiescent G0 state such as those on the left are Ki67/MKI67 negative but fibrillarin positive.](http://images.novusbio.com/fullsize/Ki67-MKI67-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-05537-img0001.jpg)
![ELISA: Apolipoprotein E/ApoE Antibody (GT27711) [NBP3-13692] - Indirect ELISA analysis performed by coating plate with recombinant full-length human apolipoprotein E (400-6.25 ng/mL). Coated protein was probed with Apolipoprotein E/ApoE antibody [GT27711] (NBP3-13692) (1 ug/mL). Mouse IgG antibody (HRP) (NBP2-19382) (1:10000) was used to detect bound primary antibody.](http://images.novusbio.com/fullsize/Apolipoprotein-E-ApoE-Antibody-GT27711-ELISA-NBP3-13692-img0001.jpg "ELISA: Apolipoprotein E/ApoE Antibody (GT27711) [NBP3-13692] - Indirect ELISA analysis performed by coating plate with recombinant full-length human apolipoprotein E (400-6.25 ng/mL). Coated protein was probed with Apolipoprotein E/ApoE antibody [GT27711] (NBP3-13692) (1 ug/mL). Mouse IgG antibody (HRP) (NBP2-19382) (1:10000) was used to detect bound primary antibody.")
![Sandwich ELISA: Apolipoprotein E/ApoE Antibody (GT27711) [NBP3-13692] - Sandwich ELISA detection of recombinant full-length human apolipoprotein E using Apolipoprotein E/ApoE antibody [GT27711] (NBP3-13692) as capture antibody at concentration of 5 ug/mL and Apolipoprotein E/ApoE antibody [C2C3], C-term as detection antibody at concentration of 1 ug/mL. Rabbit IgG antibody (HRP) (NBP2-19301) was diluted at 1:10000 and used to detect the primary antibody.](http://images.novusbio.com/fullsize/Apolipoprotein-E-ApoE-Antibody-GT27711-Sandwich-ELISA-NBP3-13692-img0002.jpg)
![Western Blot: Apolipoprotein E/ApoE Antibody (GT27711) [NBP3-13692] - Human plasma (30 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with Apolipoprotein E/ApoE antibody [GT27711] (NBP3-13692) diluted at 1:25000. The HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-13692_mouse-apolipoprotein-e-apoe-mab-gt27711-91020242075981.jpg)
![Western Blot: Apolipoprotein E/ApoE Antibody (GT27711) [NBP3-13692] - Rat plasma (50 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with Apolipoprotein E/ApoE antibody [GT27711] (NBP3-13692) diluted at 1:25000. The HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-13692_mouse-apolipoprotein-e-apoe-mab-gt27711-9102024200102.jpg)
![Apolipoprotein E antibody [GT27711] detects Apolipoprotein E protein by immunohistochemical analysis.Sample: Paraffin-embedded rat tissues.Apolipoprotein E stained by Apolipoprotein E antibody [GT27711] (NBP3-13692) diluted at 1:200.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13692_mouse-apolipoprotein-e-apoe-mab-gt27711-immunohistochemistry-paraffin-2611202518393121.jpg)
![Apolipoprotein E antibody [GT27711] detects Apolipoprotein E protein by immunohistochemical analysis.Sample: Paraffin-embedded mouse tissues.Apolipoprotein E stained by Apolipoprotein E antibody [GT27711] (NBP3-13692) diluted at 1:200.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13692_mouse-apolipoprotein-e-apoe-mab-gt27711-immunohistochemistry-paraffin-26112025182905.jpg)
![Apolipoprotein E antibody [GT27711] detects Apolipoprotein E protein by immunohistochemical analysis.Sample: Paraffin-embedded rat tissues.Apolipoprotein E stained by Apolipoprotein E antibody [GT27711] (NBP3-13692) diluted at 1:200.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13692_mouse-apolipoprotein-e-apoe-mab-gt27711-immunohistochemistry-paraffin-2611202518393113.jpg)
![Apolipoprotein E antibody [GT27711] detects Apolipoprotein E protein by immunohistochemical analysis.Sample: Paraffin-embedded human tissues.Apolipoprotein E stained by Apolipoprotein E antibody [GT27711] (NBP3-13692) diluted at 1:200.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13692_mouse-apolipoprotein-e-apoe-mab-gt27711-immunohistochemistry-paraffin-261120251992711.jpg)
![Apolipoprotein E antibody [GT27711] detects Apolipoprotein E protein by immunohistochemical analysis.Sample: Paraffin-embedded human tissues.Apolipoprotein E stained by Apolipoprotein E antibody [GT27711] (NBP3-13692) diluted at 1:200.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13692_mouse-apolipoprotein-e-apoe-mab-gt27711-immunohistochemistry-paraffin-2611202518372416.jpg)
![Western Blot: Fibrillarin Antibody [NBP3-05533] - Western blot analysis of different tissue and cell line lysates using Fibrillarin Antibody at a dilution of 1:2,000, in green: [1] protein standard (red), [2] rat whole brain, [3] mouse whole brain, [4] NIH-3T3 cells,[5] HEK293, [6] HeLa, and [7] SH-SY5Y cells. Strong band at ~35kDa corresponds to Fibrillarin protein seen in all cell line lysates. A much weaker band is seen in tissue lysates since Fibrillarin is more heavily expressed in rapidly dividing cells. The blot simultaneously was probed with rabbit pAb to UCHL1 at a dilution of 1:3,000, in red, revealing the ~25kDa UCHL1 protein in lysates of tissues containing neurons or cells with neuronal properties.](http://images.novusbio.com/fullsize/Fibrillarin-Antibody-Western-Blot-NBP3-05533-img0002.jpg "Western Blot: Fibrillarin Antibody [NBP3-05533] - Western blot analysis of different tissue and cell line lysates using Fibrillarin Antibody at a dilution of 1:2,000, in green: [1] protein standard (red), [2] rat whole brain, [3] mouse whole brain, [4] NIH-3T3 cells,[5] HEK293, [6] HeLa, and [7] SH-SY5Y cells. Strong band at ~35kDa corresponds to Fibrillarin protein seen in all cell line lysates. A much weaker band is seen in tissue lysates since Fibrillarin is more heavily expressed in rapidly dividing cells. The blot simultaneously was probed with rabbit pAb to UCHL1 at a dilution of 1:3,000, in red, revealing the ~25kDa UCHL1 protein in lysates of tissues containing neurons or cells with neuronal properties.")
![Immunocytochemistry/Immunofluorescence: Fibrillarin Antibody [NBP3-05533] - Immunofluorescent analysis of (A) C6 rat glioma cells and (B) HEK293 human embryonic kidney cells stained with Fibrillarin Antibody at a dilution of 1:1,000 in red, in both cases costained with chicken pAb to vimentin at a dilution of 1:10,000 in green. The blue is DAPI staining of nuclear DNA. The Fibrillarin antibody detects Fibrillarin protein localized in nucleoli while the vimentin antibody produces strong staining of cytoplasmic intermediate filaments.](http://images.novusbio.com/fullsize/Fibrillarin-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-05533-img0001.jpg)