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![Western Blot: CASC5 Antibody (HL2158) - Azide and BSA Free [NBP3-25397] - A431 whole cell and nuclear extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with CASC5 antibody [HL2158] (NBP3-25397) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/nbp3-25397_rabbit-casc5-mab-hl2158-azide-and-bsa-free-212024940879.jpg "Western Blot: CASC5 Antibody (HL2158) - Azide and BSA Free [NBP3-25397] - A431 whole cell and nuclear extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with CASC5 antibody [HL2158] (NBP3-25397) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.")
![Immunocytochemistry/Immunofluorescence: CASC5 Antibody (HL2158) - Azide and BSA Free [NBP3-25397] - CASC5 antibody [HL2158] detects CASC5 protein at kinetochore by immunofluorescent analysis. Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: CASC5 stained by CASC5 antibody [HL2158] (NBP3-25397) diluted at 1:500. Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [GT114] (NBP2-43837) diluted at 1:1000. Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp3-25397_rabbit-casc5-mab-hl2158-azide-and-bsa-free-212024943558.jpg)
![Western Blot: UBR5/EDD Antibody [NBP3-12948] - U87-MG whole cell and nuclear extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with UBR5/EDD antibody (NBP3-12948) diluted at 1:500.](http://images.novusbio.com/fullsize/UBR5-EDD-Antibody-Western-Blot-NBP3-12948-img0001.jpg "Western Blot: UBR5/EDD Antibody [NBP3-12948] - U87-MG whole cell and nuclear extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with UBR5/EDD antibody (NBP3-12948) diluted at 1:500.")
![EDD antibody detects EDD protein at nucleus by immunofluorescent analysis.Sample: U87-MG cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: EDD protein stained by EDD antibody (NBP3-12948) diluted at 1:500.Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [GT114] diluted at 1:1000.Blue: Hoechst 33342 staining.Scale bar = 10 um.](http://images.novusbio.com/fullsize/nbp3-12948_rabbit-ubr5-edd-pab-immunocytochemistry-immunofluorescence-261120251842320.jpg)
![Western Blot: p16INK4a/CDKN2A Antibody (GT888) [NBP3-13670] - Various whole cell extracts (30 ug) were separated by 15% SDS-PAGE, and the membrane was blotted with p16INK4a/CDKN2A antibody [888] (NBP3-13670) diluted at 1:1000. The HRP-conjugated anti-mouse IgG antibody (NBP2-19382) 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/p16INK4a-CDKN2A-Antibody-GT888-Western-Blot-NBP3-13670-img0002.jpg "Western Blot: p16INK4a/CDKN2A Antibody (GT888) [NBP3-13670] - Various whole cell extracts (30 ug) were separated by 15% SDS-PAGE, and the membrane was blotted with p16INK4a/CDKN2A antibody [888] (NBP3-13670) diluted at 1:1000. The HRP-conjugated anti-mouse IgG antibody (NBP2-19382) was used to detect the primary antibody. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.")
![Immunohistochemistry-Paraffin: p16INK4a/CDKN2A Antibody (GT888) [NBP3-13670] - Human breast. p16INK4a/CDKN2A stained by p16INK4a/CDKN2A antibody [888] (NBP3-13670) diluted at 1:200. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](http://images.novusbio.com/fullsize/p16INK4a-CDKN2A-Antibody-GT888-Immunohistochemistry-Paraffin-NBP3-13670-img0001.jpg)
![Immunohistochemistry:[NBP3-29343]-Detection of mouse Phospho-RPA32 by immunohistochemistry. Sample: FFPE section of mouse gut. Antibody: Affinity purified rabbit anti-Phospho-RPA32.](http://images.novusbio.com/fullsize/nbp3-29343_rabbit-rpa2-pab-231202511595087.jpg "Immunohistochemistry:[NBP3-29343]-Detection of mouse Phospho-RPA32 by immunohistochemistry. Sample: FFPE section of mouse gut. Antibody: Affinity purified rabbit anti-Phospho-RPA32.")
![Western Blot: MCPH1 Antibody (2A3) [NBP2-45775] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY MCPH1.](http://images.novusbio.com/fullsize/MCPH1-Antibody-2A3-Western-Blot-NBP2-45775-img0002.jpg "Western Blot: MCPH1 Antibody (2A3) [NBP2-45775] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY MCPH1.")
![Immunohistochemistry: MCPH1 Antibody (2A3) [NBP2-45775] - Analysis of Human thyroid tissue. (Heat-induced epitope retrieval by 1 mM EDTA in 10mM Tris, pH8.5, 120C for 3min)](http://images.novusbio.com/fullsize/MCPH1-Antibody-2A3-Immunohistochemistry-NBP2-45775-img0001.jpg)
![Western Blot: RFC2 Antibody (11C6) [NBP2-45569] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY RFC2.](http://images.novusbio.com/fullsize/RFC2-Antibody-11C6-Western-Blot-NBP2-45569-img0002.jpg "Western Blot: RFC2 Antibody (11C6) [NBP2-45569] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY RFC2.")
![Flow Cytometry: RFC2 Antibody (11C6) [NBP2-45569] - Analysis of HEK293T cells transfected with either overexpress plasmid(Red) or empty vector control plasmid(Blue) were immunostained by RFC2 antibody.](http://images.novusbio.com/fullsize/RFC2-Antibody-11C6-Flow-Cytometry-NBP2-45569-img0001.jpg)
![Western Blot: SHPRH Antibody (OTI5G8) [NBP2-02797] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY SHPRH (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-SHPRH.](http://images.novusbio.com/fullsize/SHPRH-Antibody-OTI5G8-Western-Blot-NBP2-02797-img0002.jpg "Western Blot: SHPRH Antibody (OTI5G8) [NBP2-02797] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY SHPRH (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-SHPRH.")
![Flow Cytometry: SHPRH Antibody (OTI5G8) [NBP2-02797] - Analysis of Jurkat cells, using anti-SHPRH antibody, (Red), compared to a nonspecific negative control antibody (Blue).](http://images.novusbio.com/fullsize/SHPRH-Antibody-OTI5G8-Flow-Cytometry-NBP2-02797-img0001.jpg)
![Immunohistochemistry-Paraffin: NEIL1 Antibody [NB300-881] - Analysis of NEIL1 in paraffin embedded Human Placenta using this antibody at 5 ug/mL. Steamed antigen retrieval with citrate buffer pH 6, AP-staining. Human placenta shows strong staining of cytoplasm in syncytiotrophoblasts.](http://images.novusbio.com/fullsize/NEIL1-Antibody-Immunohistochemistry-Paraffin-NB300-881-img0002.jpg "Immunohistochemistry-Paraffin: NEIL1 Antibody [NB300-881] - Analysis of NEIL1 in paraffin embedded Human Placenta using this antibody at 5 ug/mL. Steamed antigen retrieval with citrate buffer pH 6, AP-staining. Human placenta shows strong staining of cytoplasm in syncytiotrophoblasts.")