Anti-CNPase antibody [11-5B]

10 product images

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  Western blot - Anti-CNPase antibody [11-5B] (ab6319)

  Lanes 1 - 3: Merged signal (red and green). Green - ab6319 observed at 48 kDa. Red - loading control, Anti-GAPDH antibody [EPR16891] - Loading Control ab181602, observed at 37 kDa.
  

  ab6319 was shown to recognize CNPase in wild-type HAP1 cells as signal was lost at the expected MW in CNPase knockout cells. Additional cross-reactive bands were observed in the wild-type and knockout cells. Wild-type and CNPase knockout samples were subjected to SDS-PAGE. ab6319 and Anti-GAPDH antibody [EPR16891] - Loading Control ab181602 (Rabbit anti-GAPDH loading control) were incubated overnight at 4°C at 5 μg/ml and 1/20000 dilution respectively. Blots were developed with Goat anti-Mouse IgG H&L (IRDye^® 800CW) preabsorbed Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed ab216772 and Goat anti-Rabbit IgG H&L (IRDye^® 680RD) preabsorbed Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed ab216777 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.

  All lanes: Western blot - Anti-CNPase antibody [11-5B] (ab6319) at 5 µg/mL

  Lane 1: Wild-type HAP1 whole cell lysate at 40 µg

  Lane 2: CNPase knockout HAP1 whole cell lysate at 40 µg

  Lane 3: Human Brain whole cell lysate at 20 µg

  Predicted band size: 48 kDa

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  This image is courtesy of an anonymous customer review.

  Immunocytochemistry/ Immunofluorescence - Anti-CNPase antibody [11-5B] (ab6319)

  ab6319 staining CNPase in rat oligodendrocytes by Immunocytochemistry/ Immunofluorescence.
  
  Cells were fixed in paraformaldehyde, blocked using 5% serum for 10 minutes at 25°C, then incubated with ab6319 at a 1/200 dilution for 2 hours at 25°C. The secondary used was a goat anti-mouse Cy3 conjugated polyclonal at a 1/100 dilution.

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  Immunocytochemistry/ Immunofluorescence - Anti-CNPase antibody [11-5B] (ab6319)

  ab6319 staining CNPase in primary hippocampal rat neurons/glia, (obtained from Neuromics, cat. no. PC35101), DIV14. cells. The cells were fixed with 100% methanol (5 min), permeabilized with 0.1% PBS-Tween for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1% PBS-Tween for 1h. The cells were then incubated overnight at 4°C with ab6319 at 1µg/ml and Anti-beta Tubulin antibody - Loading Control ab6046, Rabbit polyclonal to beta Tubulin - Loading Control. Cells were then incubated with Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) preadsorbed ab150117, Goat polyclonal Secondary Antibody to Mouse IgG H&L (Alexa Fluor^® 488) preadsorbed at 1/1000 dilution (shown in green) and Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) ab150080, Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (Alexa Fluor^® 594) at 1/1000 dilution (shown in pseudocolour red). Nuclear DNA was labelled with DAPI (shown in blue).

  Also suitable in cells fixed with 4% paraformaldehyde (10 min).

  Image was acquired with a confocal microscope (Leica-Microsystems TCS SP8) and a single confocal section is shown.

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  Western blot - Anti-CNPase antibody [11-5B] (ab6319)

  Lanes 1- 2: Merged signal (red and green). Green - ab6319 observed at 48 kDa. Red - Anti-GAPDH antibody[EPR16891] - Loading Control (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) observed at 37 kDa.
  

  ab6319 was shown to react with CNPase in wild-type HeLa cells in western blot. Loss of signal was observed when knockout cell line Human CNP (CNPase) knockout HeLa cell line ab264949 (knockout cell lysate Human CNP (CNPase) knockout HeLa cell lysate ab256877) was used. Wild-type HeLa and CNP knockout HeLa cell lysates were subjected to SDS-PAGE. Membrane was blocked for 1 hour at room temperature in 0.1% TBST with 3% non-fat dried milk. ab6319 and Anti-GAPDH antibody [EPR16891] - Loading Control (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) overnight at 4°C at 5 μg/ml and a 1 in 20000 dilution respectively. Blots were developed with Goat anti-Mouse IgG H&L (IRDye^®800CW) preadsorbed (Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed ab216772) and Goat Anti-Rabbit IgG H&L (IRDye^®680RD) preadsorbed (Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed ab216777) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.

  All lanes: Western blot - Anti-CNPase antibody [11-5B] (ab6319) at 5 µg/mL

  Lane 1: Wild-type HeLa cell lysate at 20 µg

  Lane 1: Western blot - Human CNP (CNPase) knockout HeLa cell pellet (Human CNP (CNPase) knockout HeLa cell pellet ab278945)

  Lane 1: Western blot - Human CNP (CNPase) knockout HeLa cell lysate (Human CNP (CNPase) knockout HeLa cell lysate ab256877)

  Lane 2: CNP knockout HeLa cell lysate at 20 µg

  Lane 2: Western blot - Human CNP (CNPase) knockout HeLa cell line (Human CNP (CNPase) knockout HeLa cell line ab264949)

  Performed under reducing conditions.

  Predicted band size: 48 kDa

  Observed band size: 48 kDa

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  This image is courtesy of a customer review submitted by Carl Hobbs, King's College London, United Kingdom

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CNPase antibody [11-5B] (ab6319)

  IHC-P image of CNPase staining on rat brain sections using ab6319 (1/1600). heat mediated antigen retrieval on paraffin embedded sections was performed using citric acid. The sections were then blocked with 1% BSA for 10 min at 21°C. The primary antibody was incubated for 16 hours at 21°C. The sections were then incubated in Goat anti-mouse (Biotin) at 1:200.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CNPase antibody [11-5B] (ab6319)

  IHC image of CNPase staining in human cerebral cortex formalin fixed paraffin embedded tissue section, performed on a Leica Bond™ system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab6319, 5μg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

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  This image is courtesy of an anonymous customer review

  Immunocytochemistry/ Immunofluorescence - Anti-CNPase antibody [11-5B] (ab6319)

  ab6319 staining CNPase in the rat oligodendrocytes by ICC/IF (Immunoytochemistry/immunofluorescence). Cells were fixed with paraformaldehyde, permeabilized with methanol and blocked with 5% BSA for 1 hour at 37°C. Samples were incubated with primary antibody (1/100 in PBS) for 18 hours at 4°C. An Alexa Fluor^® 594-conjugated Goat anti-mouse IgG polyclonal (1:200) was used as the secondary antibody.

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  This image is courtesy of an anonymous customer review

  Western blot - Anti-CNPase antibody [11-5B] (ab6319)

  All lanes: Western blot - Anti-CNPase antibody [11-5B] (ab6319) at 1/750 dilution

  All lanes: Spinal Cord homogenate (whole tissue lysate) at 2 µg

  Secondary

  All lanes: HRP conjugated sheep anti-mouse IgG

  Predicted band size: 48 kDa

  Observed band size: 45 kDa, 47 kDa

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  This image is courtesy of a customer review submitted by Carl Hobbs, King's College London, United Kingdom

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CNPase antibody [11-5B] (ab6319)

  ab6319 staining CNPase in Dog Cerebellum tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with formaldehyde and blocked with 1% BSA for 10 minutes at 21°C; antigen retrieval was by heat mediation in a citrate buffer. Samples were incubated with primary antibody (1/1500 in blocking buffer) for 2 hours at 21°C. A Biotin-conjugated Goat anti-mouset IgG polyclonal (1/200) was used as the secondary antibody.

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  Western blot - Anti-CNPase antibody [11-5B] (ab6319)

  This antibody was raised against full length native CNPase and is predicted to recognize both isoforms. The predicted molecular weights of isoforms CNPI and CNPII are 45- and 48-kDa respectively.

  All lanes: Western blot - Anti-CNPase antibody [11-5B] (ab6319) at 1/100 dilution

  Lane 1: Human spinal cord tissue lysate - total protein (ab29188) at 20 µg

  Lane 2: Human brain tissue lysate - total protein (ab29466) at 20 µg

  Lane 3: Spinal Cord (Mouse) Tissue Lysate at 20 µg

  Lane 4: Brain (Mouse) Tissue Lysate at 20 µg

  Lane 5: Spinal Cord (Rat) Tissue Lysate at 20 µg

  Lane 6: Brain (Rat) Tissue Lysate at 20 µg

  Secondary

  All lanes: Goat polyclonal to Mouse IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution

  Developed using the ECL technique.

  Performed under reducing conditions.

  Predicted band size: 48 kDa

  Exposure time: 1min