Note: Mouseover a species abbreviation on the product page to display the fullname.
How can we help you?
![Flow Cytometry: CD45RO Antibody (ILA116A) [NBP2-61035] - Obtained with bovine leukocytes](http://images.novusbio.com/fullsize/CD45RO-Antibody-ILA116A-Flow-Cytometry-NBP2-61035-img0001.jpg "Flow Cytometry: CD45RO Antibody (ILA116A) [NBP2-61035] - Obtained with bovine leukocytes")
![Western Blot: Nicotinic Acetylcholine Receptor beta 2 Antibody (1C7) [H00001141-M01] - CHRNB2 monoclonal antibody (M01), clone 1C7. Analysis of CHRNB2 expression in rat testis.](http://images.novusbio.com/fullsize/Nicotinic-Acetylcholine-Receptor-beta-2-Antibody-1C7-Western-Blot-H00001141-M01-img0001.jpg "Western Blot: Nicotinic Acetylcholine Receptor beta 2 Antibody (1C7) [H00001141-M01] - CHRNB2 monoclonal antibody (M01), clone 1C7. Analysis of CHRNB2 expression in rat testis.")
![SH3PXD2A antibody [GT88] detects SH3PXD2A protein by immunohistochemical analysis.Sample: Paraffin-embedded mouse tissues.SH3PXD2A stained by SH3PXD2A antibody [GT88] (NBP3-48845) diluted at 1:200.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-48845_mouse-sh3pxd2a-mab-gt88-immunohistochemistry-paraffin-141120251838410.jpg "<b>Orthogonal Strategies Validation. </b>SH3PXD2A antibody [GT88] detects SH3PXD2A protein by immunohistochemical analysis.Sample: Paraffin-embedded mouse tissues.SH3PXD2A stained by SH3PXD2A antibody [GT88] (NBP3-48845) diluted at 1:200.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min")
![Immunohistochemistry-Paraffin: VLDLR Antibody (rVLDLR/1337) [NBP3-13794] - Formalin-fixed, paraffin-embedded human pancreas stained with VLDLR antibody (rVLDLR/1337). Inset: PBS instead of primary antibody; secondary only negative control.](http://images.novusbio.com/fullsize/VLDLR-Antibody-rVLDLR-1337-Immunohistochemistry-Paraffin-NBP3-13794-img0001.jpg "Immunohistochemistry-Paraffin: VLDLR Antibody (rVLDLR/1337) [NBP3-13794] - Formalin-fixed, paraffin-embedded human pancreas stained with VLDLR antibody (rVLDLR/1337). Inset: PBS instead of primary antibody; secondary only negative control.")
![ELISA: Malondialdehyde ELISA Kit (Colorimetric) [NBP2-78753] - Samples were spiked with high concentrations of Malondialdehyde and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.](http://images.novusbio.com/fullsize/nbp2-78753_malondialdehyde-elisa-kit-colorimetric-132202416175629.jpg "ELISA: Malondialdehyde ELISA Kit (Colorimetric) [NBP2-78753] - Samples were spiked with high concentrations of Malondialdehyde and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.")
![ELISA: Malondialdehyde ELISA Kit (Colorimetric) [NBP2-78753] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp2-78753_malondialdehyde-elisa-kit-colorimetric-4320249124814.jpg)
![Western Blot: TOMM40 Antibody [NBP3-13290] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with TOMM40 antibody (NBP3-13290) 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/TOMM40-Antibody-Western-Blot-NBP3-13290-img0001.jpg "Western Blot: TOMM40 Antibody [NBP3-13290] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with TOMM40 antibody (NBP3-13290) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Western Blot: alpha Adaptin Antibody [NBP3-13154] - Whole cell extract (30 ug) was separated by 5% SDS-PAGE, and the membrane was blotted with alpha Adaptin antibody (NBP3-13154) 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/alpha-Adaptin-Antibody-Western-Blot-NBP3-13154-img0001.jpg "Western Blot: alpha Adaptin Antibody [NBP3-13154] - Whole cell extract (30 ug) was separated by 5% SDS-PAGE, and the membrane was blotted with alpha Adaptin antibody (NBP3-13154) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Western Blot: CLN5 Antibody [NBP3-12971] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with CLN5 antibody (NBP3-12971) diluted at 1:1000.](http://images.novusbio.com/fullsize/CLN5-Antibody-Western-Blot-NBP3-12971-img0001.jpg "Western Blot: CLN5 Antibody [NBP3-12971] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with CLN5 antibody (NBP3-12971) diluted at 1:1000.")
![Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with HFE antibody [HL2155] (NBP3-48673) diluted at 1:1000. 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/nbp3-48673_rabbit-hfe-mab-hl2155-western-blot-1411202518243315.jpg "<b>Orthogonal Strategies Validation. </b>Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with HFE antibody [HL2155] (NBP3-48673) diluted at 1:1000. 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.")
![Untreated (–) and treated (+) SH-SY5Y whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membranes were blotted with Tau (pSer235) antibody (HL3899) diluted at 1:1000 and Tau antibody [HL2982] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-45162_rabbit-tau-p-ser235-mab-hl3899-azide-and-bsa-free-western-blot-2942025155710..jpg "<b>Biological Strategies Validation. </b>Untreated (–) and treated (+) SH-SY5Y whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membranes were blotted with Tau (pSer235) antibody (HL3899) diluted at 1:1000 and Tau antibody [HL2982] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")