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![Western Blot: Apolipoprotein H/ApoH Antibody (H219) [NBP3-18286] - Detection of human Apolipoprotein H/ApoH with NBP3-18286 in Western blot. Human plasma (0.1 ul and 0.01 ul) in SDS sample buffer were denatured at 70C for 10 minutes and run on SDS-page / Western blot. Apolipoprotein H/ApoH was detected using 1 ug/ml H219 (biotinylated) followed by SA-ALP and BCIP/NBT-plus substrate.](http://images.novusbio.com/fullsize/Apolipoprotein-H-ApoH-Antibody-H219-Western-Blot-NBP3-18286-img0001.jpg "Western Blot: Apolipoprotein H/ApoH Antibody (H219) [NBP3-18286] - Detection of human Apolipoprotein H/ApoH with NBP3-18286 in Western blot. Human plasma (0.1 ul and 0.01 ul) in SDS sample buffer were denatured at 70C for 10 minutes and run on SDS-page / Western blot. Apolipoprotein H/ApoH was detected using 1 ug/ml H219 (biotinylated) followed by SA-ALP and BCIP/NBT-plus substrate.")
![Western Blot: Monoglyceride Lipase Antibody (HL1937) - Azide and BSA Free [NBP3-25378] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Monoglyceride lipase antibody [HL1937] (NBP3-25378) 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. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.](http://images.novusbio.com/fullsize/nbp3-25378_rabbit-monoglyceride-lipase-mab-hl1937-azide-bsa-free-2120249425450.jpg "<b>Orthogonal Strategies Validation. </b>Western Blot: Monoglyceride Lipase Antibody (HL1937) - Azide and BSA Free [NBP3-25378] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Monoglyceride lipase antibody [HL1937] (NBP3-25378) 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. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.")
![Western Blot: IGF-I R/IGF1R [p Tyr1146] Antibody [NBP3-13236] - Untreated (-) and treated (+) MCF-7 whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with IGF1R (phospho Tyr1131) / Insulin Receptor (phospho Tyr1146) antibody (NBP3-13236) 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/IGF-I-R-IGF1R-[p-Tyr1146]-Antibody-Western-Blot-NBP3-13236-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: IGF-I R/IGF1R [p Tyr1146] Antibody [NBP3-13236] - Untreated (-) and treated (+) MCF-7 whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with IGF1R (phospho Tyr1131) / Insulin Receptor (phospho Tyr1146) antibody (NBP3-13236) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunohistochemistry-Frozen: GIRK2 Antibody [NBP3-13346] - GIRK2 antibody detects GIRK2 protein by immunohistochemical analysis. Sample: Frozen-sectioned mouse cerebellum. Green: GIRK2 stained by GIRK2 antibody (NBP3-13346) diluted at 1:250. Red: NF-H, stained by NF-H antibody [GT114] diluted at 1:500. Blue: Fluoroshield with DAPI.](http://images.novusbio.com/fullsize/GIRK2-Antibody-Immunohistochemistry-Frozen-NBP3-13346-img0001.jpg "Immunohistochemistry-Frozen: GIRK2 Antibody [NBP3-13346] - GIRK2 antibody detects GIRK2 protein by immunohistochemical analysis. Sample: Frozen-sectioned mouse cerebellum. Green: GIRK2 stained by GIRK2 antibody (NBP3-13346) diluted at 1:250. Red: NF-H, stained by NF-H antibody [GT114] diluted at 1:500. Blue: Fluoroshield with DAPI.")
![Western Blot: PKM2 [p Ser37] Antibody [NBP3-13307] - Whole cell extract (30 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with PKM2 (phospho Ser37) antibody (NBP3-13307) 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/PKM2-[p-Ser37]-Antibody-Western-Blot-NBP3-13307-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: PKM2 [p Ser37] Antibody [NBP3-13307] - Whole cell extract (30 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with PKM2 (phospho Ser37) antibody (NBP3-13307) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Western Blot: PLC-gamma 1 [p Ser1248] Antibody [NBP3-13242] - Untreated (-) and treated (+) A431 whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with PLC-gamma 1 (phospho Ser1248) antibody (NBP3-13242) 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/PLC-gamma-1-[p-Ser1248]-Antibody-Western-Blot-NBP3-13242-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: PLC-gamma 1 [p Ser1248] Antibody [NBP3-13242] - Untreated (-) and treated (+) A431 whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with PLC-gamma 1 (phospho Ser1248) antibody (NBP3-13242) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Western Blot: PLC-gamma 2 [p Tyr759] Antibody [NBP3-13241] - Untreated (-) and treated (+) Raji whole cell extracts (10 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with PLC-gamma 2 (phospho Tyr759) antibody (NBP3-13241) 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/PLC-gamma-2-[p-Tyr759]-Antibody-Western-Blot-NBP3-13241-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: PLC-gamma 2 [p Tyr759] Antibody [NBP3-13241] - Untreated (-) and treated (+) Raji whole cell extracts (10 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with PLC-gamma 2 (phospho Tyr759) antibody (NBP3-13241) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Western Blot: EDEM1 Antibody [NBP3-12935] - Jurkat whole cell and membrane extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with EDEM1 antibody (NBP3-12935) diluted at 1:1000.](http://images.novusbio.com/fullsize/EDEM1-Antibody-Western-Blot-NBP3-12935-img0001.jpg "Western Blot: EDEM1 Antibody [NBP3-12935] - Jurkat whole cell and membrane extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with EDEM1 antibody (NBP3-12935) diluted at 1:1000.")
![Immunohistochemistry-Paraffin: Carbonic Anhydrase IX/CA9 Antibody (CA9/2993R) [NBP3-07871] - Formalin-fixed, paraffin-embedded human Renal Cell Carcinoma stained with Carbonic Anhydrase IX/CA9 Rabbit Recombinant Monoclonal Antibody (CA9/2993R).](http://images.novusbio.com/fullsize/Carbonic-Anhydrase-IX-CA9-Antibody-CA9-2993R-Immunohistochemistry-Paraffin-NBP3-07871-img0001.jpg "Immunohistochemistry-Paraffin: Carbonic Anhydrase IX/CA9 Antibody (CA9/2993R) [NBP3-07871] - Formalin-fixed, paraffin-embedded human Renal Cell Carcinoma stained with Carbonic Anhydrase IX/CA9 Rabbit Recombinant Monoclonal Antibody (CA9/2993R).")
![Western Blot: PRAS40 [p Ser183] Antibody [NBP3-13077] - Untreated (-) and treated (+) 293T whole cell extracts (40 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with PRAS40 (phospho Ser183) antibody (NBP3-13077) 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/PRAS40-[p-Ser183]-Antibody-Western-Blot-NBP3-13077-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: PRAS40 [p Ser183] Antibody [NBP3-13077] - Untreated (-) and treated (+) 293T whole cell extracts (40 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with PRAS40 (phospho Ser183) antibody (NBP3-13077) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Western Blot: IRE1 alpha [p Ser724] Antibody [NBP3-12123] - Untreated (-) and treated (+) HeLa whole cell extracts (5 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with IRE1 (phospho Ser724) antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/IRE1-alpha-[p-Ser724]-Antibody-Western-Blot-NBP3-12123-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: IRE1 alpha [p Ser724] Antibody [NBP3-12123] - Untreated (-) and treated (+) HeLa whole cell extracts (5 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with IRE1 (phospho Ser724) antibody diluted at 1:1000.")
![Western Blot: GSK-3 beta [p Ser390] Antibody [NBP3-13303] - Untreated (-) and treated (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with GSK-3 beta (phospho Thr390) antibody (NBP3-13303) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/GSK-3-beta-[p-Ser390]-Antibody-Western-Blot-NBP3-13303-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: GSK-3 beta [p Ser390] Antibody [NBP3-13303] - Untreated (-) and treated (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with GSK-3 beta (phospho Thr390) antibody (NBP3-13303) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")