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That sounds great. Please send the replacement vial to the same address as the one for the original vial. I will hopefully have better luck with this replacement. I will contact you again if I am having trouble with the replacement vial. Thanks again. |
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ANSWER: |
Thank you for confirming these details and for your cooperation. I am sorry this product did not perform as stated on the datasheet and for the inconvenience this has caused. As requested, I have issued a free of charge replacement with the order number 1065154. |
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Thank you for being very attentive to my response. Would it be possible toreceivea vial of the antibody of a different batch in a new purification but also receive a new vial of a different lot number (once it becomes available in stock) if the antibody of the different batch produces the same results as the last one and does not work? Please let me know. |
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ANSWER: |
Thank you for your quick reply. |
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I have attached pictures that I have taken of 20 micron rat brain sections stained with abcam's anti-BDNF. They are viewed under 50X and 200X and are labeled as so. The pictures I have attached are those of 1 day incubation (1-200 and 1-1000 dilutions) and 2 day incubation (1-200 and 1-1000 dilutions). I also have 3 day incubation sections that I have taken but not have attached in this email. Let me know if you would like to see those as well. |
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ANSWER: |
Thank you for taking time to provide all these images and for contacting us. I am sorry to hear and see now thatthis antibody is not providing satisfactory results. |
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Phone call: Customer uses this antibody on rat brain perfusion fixed samples. There is no specific staining, just backgound. |
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ANSWER: |
Thank you for calling us and for alerting us to the problem you are experiencing with our product. We take product complaints very seriously, and investigate every product that we feel may not be performing correctly. |
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I want to work with the next primary antibodies for ICC/IF,I wonder if I can use them on rats: |
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ANSWER: |
Thank you for contacting Abcam and for your interest in our products. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
ab6201 BDNF antibody immunostaining in the ventral horn of the spinal cord. Protocol: free floating, PFA/picric acid perfusion fixed rat coronal sections (30 microns) were incubated overnight in ab6201 (1/500) followed by 1 night of postfixation). Immunofluorescence was visualised with TSA amplification.
Sophie Pezet, King`s college London, United Kingdom
ab6201 BDNF antibody immunostaining BDNF-containing hippocampal neurons. Protocol: PFA(only)-fixed free floating coronal rat brain sections (30 microns) were incubated for 3 days with ab6201 at 1/100 followed by direct immunofluorescence detection (alexa488; 1/1000). We recommend using an amplification IHC protocol following PFA/picric acid fixation of brain tissue for optimising BDNF detection using ab6201
Sophie Pezet, King`s college London, United Kingdom
ICC/IF image of ab6201 stained PC12 cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab6201, 5µg/ml) overnight at +4ºC. 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) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
Anti-BDNF antibody (ab6201) at 1 µg/ml +
Secondary
Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (HRP), pre-adsorbed (ab97080) at 1/5000 dilution
developed using the ECL technique
Performed under reducing conditions.
Exposure time : 4 minutes
0
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