You have changed your country from  to  . Please be aware that this will change the currency in the purchasing process.

Anti-TIMP1 antibody (ab61224)

CodeSizePriceAbpointsAvailability
    
 
  • -

  •   
  •   
  •   
  •  

  •  
  •  
  •  

  •  
Updating...

Reassurance, Refunds & Replacements

If your product does not perform as described on this datasheet, we will refund or replace your product...

Read our guarantee »

This product is covered by the Abpromise guarantee. Our scientific support team are available to answer any questions or queries - fill out an inquiry form for ab61224 for help.

Alternatively, you can search the previous enquiries about this product to see if your query has already been answered.

7 questions for ab61224

first page       

Page 1 of 2

      

Question 1

Thursday 29-March-2012

What is the immunogen sequency for ab61224?

In regards to ab1827, is the whole TIMP1 human protein used as the immunogen?

ANSWER:

 

Thank you for contacting Abcam.


Regarding ab1827 the full length protein was used as an immunogen.


Regarding ab61224, it is a peptide from the central region of the protein. The specific sequence is proprietary.


I hope this information is helpful. Please do not hesitate to contact us if you have any additional questions.

Question 2

Wednesday 28-March-2012

I need to be informed about the imunogen sequence used to obtain the antibody Abcam herein specified:
Anti-TIMP1 antibody (ab61224)
Concerning Anti-TIMP1 antibody [102D1] (ab1827) is it against the whole sequence of human TIMP1?
Thanks for attention.
Sincerely yours,

ANSWER:

 

Thank you for contacting us.

The immunogen for ab61224 correspond to thecentral region of human TIMP1. The full protein sequence can be found by clicking the link; http://www.uniprot.org/uniprot/P01033

The ab1827 is against the whole sequence of human TIMP1. The exact epitope of this antibody hasn't beendetermined yet.

I hope this information is helpful to you. Please do not hesitate to contact us if you need any more advice or information.

Question 3

Friday 09-December-2011

A replacement would be great and then I will likely order a large amount in the future.  Do I need to place an order or will you place the replacement order? Thanks so much for your help!  

ANSWER:

 

Thank you for confirming these details and for your cooperation. The details provided enable us to closely monitor the quality of our products. 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. To check the status of the order please contact our Customer Service team and reference this number. Please note that this free of charge replacement vial is also covered by our Abpromise guarantee. Should you still be experiencing difficulties, or if you have any further questions, please do not hesitate to let us know. I wish you the best of luck with your research.

Question 4

Thursday 08-December-2011

I tried both TIMP antibodies at 1:1000, 1:500, and 1:100. I only got them to work at 1:100 with an overnight exposure. The control antibody I used that detects viral protein was easily detectable. I didn't quantify the amount of protein that I loaded, but I loaded the maximum 15ul volume. I included other samples on the same gel prepared the same way and they were easily detectable via WB using other antibodies.

Block: 5% milk, .1% Tween-20 in PBS Wash: 1% milk, .1% Tween-20 in PBS Blocking and AB exposure

1. Trim and mark ladder 2. Wash the membrane in PBS 3. Block 2x 40' RT 4. Wash 2x 5 min in wash 5. Incubate in primary AB diluted in wash O/N 4 degrees 6. Wash 4x 10min in wash 7. Incubate in secondary AB diluted in wash 1 hr RT 8. Wash 4x 10 min in wash 9. Place in PBS 10. Develop

I also tried ICC on transfected cells where both antibodies only worked at a 1:10 dilution with the following protocol: 1. Wash in PBS 2. Fix in 4% PFA in PBS 15' RT 3. Wash 3 times in PBS 4. Incubate in blocking solution for 15 min at RT 5. Wash with perm sol. 6. Incubate in perm sol. 15 min at RT 7. Incubate in primary antibody (dilute in perm sol) for 1.5hrs at RT 8. 3x 5 min washes in perm sol. 9. Incubate in secondary antibody for 1.5hrs at RT (dilute in perm. sol.). Cover with foil to protect from light from this point on. 10. 3x 5 min washes in perm sol. 1 1. Incubate in DAPI 1:10,000 in PBS for 10 min at RT 12. Wash with PBS 13. Add vectashield and mount Blocking solution PBS with 3% BSA and .01% sodium azide Permeablization solution PBS with 1% BSA, .1% TritonX-100, .01% sodium azide

ANSWER:

 

Thank you for taking the time to send me your protocols relating to this issue. I have been able to review them and agree that the problem here is the product.

I would like to offer you free of charge replacements for ab1828 and ab61224. I may also offer you a credit note/refund that may be used against this or any outstanding invoices.

As you have mentioned before that you will be using alot of this antibody for future experiments, I thought I might inform you that Abcam will discount orders above 5 units.

Please let me know how you would like to procceed and do not hesitate to contact us with further questions or if there are other ways in which we might help you reach your research goals.  

Question 5

Tuesday 06-December-2011

I purchased a TMIP-2 antibody (ab1828) where the recommended WB

concentration was 1:1000. I was only able to detect TIMP-2

overexpressed in cell lysates using the antibody at 1:100

concentration.

I also purchased a TIMP-1 antibody (ab61224) where the recommended WB

concentration was 1:500-1:1000. I was only able to detect TIMP-1

overexpressed in cell lysates using the antibody at 1:100

concentration and the antibody did not detect endogenous TIMP-1 in 293

cells (the suggested positive control).

Since the antibodies did not work as well as suggested, would it be

possible for me to order them again at a discounted price since I have

to use so much antibody for it to

ANSWER:

 

Thank you for contacting Abcam in regards to ab1828 and ab61224. I am sorry that you found that these products do not perform as well as expected in your applications. 

I would appreciate it if you could provide me with protocol details of the approach that you are using so that I can better determine potential reasons for the reduced performance of these antibodies. I am also very interested in the method of sample preparation that you have used. I would like to offer you assistance if possible for resolving these issues in your experiments. Could you please send me the protocols that you have used for each?  

Could you also send the lot numbers for the antibodies and a order number or PO ?

Could you also confirm the species of the tissue tested? If we cannot resolve these issues with you I would be happy to offer you a replacement or credit.  

first page       

Page 1 of 2

      

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"