Aves Labs

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Beta-Amyloid-positive “neuritic plaque” (shown in higher magnification) in cerebral cortex as seen in a post-mortum specimen taken from an Alzheimer’s disease patient. Picture courtesy of Dr. Randy Woltjer, Oregon Health & Sciences University.Immunohistochemistry of a capillary showing beta-amyloid peptide in the wall of the vessel. Paraffin-embedded section of a human brain from a patient with diagnosed Alzheimer's Disease. Primary antibody -- 1:500; secondary antibody -- 1:1000 HRP-Goat anti-chicken IgY (Aves Labs). Dr. Randy Woltjer, Dept Pathology, OHSU
Immunofluorescent staining of HeLa cells using 2 µg/mL Aves Labs chicken anti-Calnexin (CANX) (Cat. No. CANX-0100) antibody (green). Actin filaments were stained using Phalloidin (red). DAPI nuclear stain (blue) shows cell nuclei. The cells were mounted with Antibodies Incorporated Fluoroshield with DAPI mounting medium (Cat. No. AR-6501). Anti-Calnexin specifically stains the Endoplasmic Reticulum in HeLa cells. ​Western blotting of various cell lysates with Aves Labs chicken anti-Calnexin (CANX) antibody (0.05 µg/ml) and detected with anti-chicken HRP. Aves Labs Chicken anti-Calnexin recognizes endogenous Calnexin in all the cell lysates at ~90 kDa.
Aves Labs Anti-Calnexin Antibody
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HeLa cells were subjected to immunofluorescent staining using chicken anti-TOMM20 antibody (visualized in green) and Antibodies Inc mouse anti-Mortalin antibody (75-127) (visualized in red). DAPI nuclear stain (blue) shows cell nuclei. The cells were mounted with ICT's Fluoroshield with DAPI mounting medium (AR-6501). The staining revealed a complete overlap between the signal from the chicken anti-TOMM20 antibody and the mouse anti-Mortalin antibody specifically in the cell mitochondria.Western blotting of various cell lysates with chicken anti-TOMM20 antibody (0.2 µg/ml)(1:1000) and detected with anti-chicken HRP. Chicken anti-TOMM20 recognizes endogenous TOMM20 in all the cell lysates at ~16 kDa.
Aves Labs Anti-TOMM20 Antibody
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Immunofluoresence of COS7 cells expressing mScarlet3 using chicken anti-mScarlet3 antibody (green) and showing mScarlet3 autofluorescence (red). The cells were mounted with ICT's Fluoroshield with DAPI mounting medium (Cat. AR-6501). The DAPI nuclear stain (blue) shows the nuclei of both transfected and untransfected cells. The staining revealed a complete overlap between the signal from chicken anti-mScarlet3 antibody and mScarlet3 autofluoresence in transfected cells.Western blotting of mock or mScarlet3 transfected COS-7 cell lysates with chicken anti-mScarlet3 antibody (0.5 ug/ml) and detected with anti-chicken HRP. Chicken anti-mScarlet3 recognizes exogenous mScarlet3 in COS-7 cells.​
Aves Labs Anti-mScarlet3 Antibody
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Immunofluorescent staining of MCF7 cells using 1 µg/mL chicken anti-HB9 (MNX1) antibody (green). Actin filaments were stained using Phalloidin (red). The cells were mounted with ICT's Fluoroshield mounting medium (Cat no. AR-6500). Anti-HB9/MNX1 specifically stains the nucleus of MCF7 cells.​Western blotting of MCF7 cell lysates with  chicken anti-HB9 (MNX1) antibody at various concentrations and detected with anti-chicken HRP. Chicken anti-HB9/MNX1 recognizes endogenous MNX1 in MCF7 cell lysates at ~50 kDa.
Aves Labs Anti-MNX1/HB9 Antibody
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