Products:Neuroscience >> Neurotransmission >> Intracellular Signaling >> Adapters
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ab18661 |
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Thank you for the quick reply Jeremy. It was very helpful. |
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ANSWER: |
I'm happy to help! Please let me know if you have any other questions. |
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To whom it may concern, |
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ANSWER: |
Thank you for your enquiry. |
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ANSWER: |
Thank you very much for your interest in ab18258. |
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Hi, |
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ANSWER: |
Thank you for contacting us. I apologise for keeping you waiting. |
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To whom it may concern, I am the process of writing a paper and wanted to know what the PSD-95 antibody (ab18258) was raised against. Was it near the N-terminal end or C-terminal end of the PSD-95 mouse peptide? |
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ANSWER: |
Thank you for contacting Abcam. The PSD95 antibody, ab18258 was generated to the N-terminal region of mouse. I hope the paper writing goes well and if you have any other questions please do not hesitate to contact us. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
All lanes : Anti-PSD95 antibody - Synaptic Marker (ab18258) at 1 µg/ml
Lane 1 : wildtype mouse brain tissue lysate
Lane 2 : PSD95 knockout mouse brain tissue lysate
Lysates/proteins at 20 µg per lane.
Performed under reducing conditions.
Predicted band size : 80 kDa
Observed band size : ~80 kDa (why is the actual band size different from the predicted?)
Lane 1 - Input lane 500ug mouse brain lysate
Lane 2 - IP lane 50ug mouse brain lysate
NB: as expected, an enrichment of PSD95 protein is observed in the IP lane.
Chris Anderson, Wellcome Trust Sanger Institute, United Kingdom
All lanes : Anti-PSD95 antibody - Synaptic Marker (ab18258) at 1 µg/ml
Lane 1 : Brain (Mouse) Tissue Lysate (ab27253)
Lane 2 : Brain (Rat) Tissue Lysate (ab7942)
Lysates/proteins at 10 µg per lane.
Secondary
IRDye 680 Conjugated Goat Anti-Rabbit IgG (H+L) (ab28446) at 1/10000 dilution
Performed under reducing conditions.
Predicted band size : 80 kDa
Observed band size : 85 kDa (why is the actual band size different from the predicted?)
ab18258 (1/1000) staining PSD9 in paraffin-embedded rat cerebellum. Tissue was fixed in formaldehyde, blocking performed using 1% BSA (10 mins/RT) and heat mediated antigen retrieval performed before staining. The secondary antibody (1/200) was goat anti rabbit IgG conjugated to Biotin. For further experimental details please refer to abreview.
Carl Hobbs, King`s College London, United Kingdom
ab18258 (1/500) staining PSD95 in paraffin-embedded Mouse Cerebellum (Top) and Medulla (Bottom) tissue, showing positive staining to the synaptic regions of the brain. Tissue was fixed in formaldehyde, blocking performed using 1% BSA (10 mins/RT) and heat mediated antigen retrieval performed before staining. The secondary antibody (1/200) was goat anti rabbit IgG conjugated to Biotin. For further experimental details please refer to abreview.
This image is courtesy of an abreview submitted by Carl Hobbs
ab18258 staining PSD95 in murine retinal tissue by Immunohistochemistry (Frozen sections).Tissue was fixed with paraformaldehyde, blocked using 10% serum for 30 minutes at 24°C, then incubated with ab18258 at a 1/1000 dilution for 16 hours at 4°C. The secondary used was an Alexa Fluor 488 conjugated goat anti-rabbit polyclonal used at a 1/1000 dilution.
Image courtesy of an anonymous Abreview.
ab18258 staining PSD95 in rat retinal tissue by Immunohistochemistry (Frozen sections).Tissue was fixed with paraformaldehyde, blocked using 10% serum for 30 minutes at 24°C, then incubated with ab18258 at a 1/1000 dilution for 16 hours at 4°C. The secondary used was an Alexa Fluor 488 conjugated goat anti-rabbit polyclonal used at a 1/1000 dilution.
Image courtesy of an anonymous Abreview.
ab18258 staining PSD95 in human SH-SY5Y cells by Immunocytochemistry/ Immunofluorescence.Cells were fixed in paraformaldehyde, blocked with 10% serum for 20 minutes at 24°C, then incubated with ab18258 at a 1/1000 dilution for 16 hours at 4°C. The secondary used was an Alexa-Fluor 488 conjugated donkey anti-rabbit polyclonal used at a 1/1000 dilution. Counterstained with Hoechst 33258 (blue).
Image courtesy of an anonymous Abreview.
ICC/IF image of ab18258 stained human SHSY5Y cells. The cells were 4% PFA fixed (10 min), permabilised in 0.1% PBS-Tween (20 min) and incubated with the antibody (ab18258, 1µg/ml) for 1h at room temperature. 1%BSA / 10% normal goat serum / 0.3M glycine was used to block non-specific protein-protein interactions. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red). DAPI was used to stain the cell nuclei (blue).
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