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Custom panel

Sample profiling service

Our teams are on hand to reply to your inquiry or you can call us with any requirements and feedback.

We look forward to hearing from you.

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  13. Please describe the problem experienced and tell us as much information as possible about your experiment (description of problem, sample preparation and species, experimental conditions, controls used, any troubleshooting you have attempted, whether this product has been used successfully in the past), including:
  14. Custom panel request

    Profiling service request

    Please give as much information as possible. We will contact you to follow up.

  15. The more information you provide, the easier it will be for us to assist with your inquiry…

    Product type, species, quantity etc.

    Please tell us as much information as possible about your experiment ; the conditions, the controls, any troubleshooting tips that you have attempted …. E.g.

    • Sample preparation
    • Electrophoresis and transfer conditions
    • Blocking conditions
    • Primary antibody conditions
    • Secondary antibody conditions
    • Wash steps
    • Detection
    Interested in larger quantities? Contact us for a quote.
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    If you have excellent quality products, we'd be delighted to market and distribute these for you.
    e.g. brief description of study, key questions.
    e.g. brief description of study, how many samples, quantity of sample available.
    e.g. how many samples, quantity of sample available, brief description of study, time frame of study.
    ChIP
    • DNA detection method (regions amplified in PCR, microarray, direct sequencing)
    • DNA purification (decrosslinking conditions, DNA purification method)
    • Immunoprecipitation conditions (buffer, amount of detergent, primary antibody manufacturer/dilution, incubation time, matrix for isolating antibody complex)
    • Sample preparation (X-ChIP/N-ChIP, cross-linking conditions, DNA fragment size)
    • Wash steps
    ELISA
    • Amount of protein used
    • Blocking conditions
    • Detection method
    • Primary antibody conditions (diluent/dilution, incubation time/temperature)
    • Secondary antibody conditions (diluent/dilution, incubation time/temperature)
    • Type of ELISA (e.g. direct, indirect, sandwich ELISA)
    • Wash steps
    • What did the standard curve look like?
    Flow Cytometry
    • Blocking/fixation conditions
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    • Number of cells used
    • Primary antibody conditions (diluent/dilution, incubation time/temperature)
    • Secondary antibody conditions (diluent/dilution, incubation time/temperature)
    • Wash steps
    Kit
    • Primary antibody conjugation conditions (amount, isotype, buffer, incubation time/temperature)
    • Sample preparation, treatment(s) (sample type, method of protein removal)
    • Storage conditions of kit components
    • Was the exact protocol followed (as supplied with the kit)?
    • Which kit component is causing the issue (enzyme/developer/standard)
    IHC
    • Blocking conditions
    • Detection method, amplification steps (if any)
    • Primary antibody conditions (diluent/dilution, incubation time/temperature)
    • Sample fixation, antigen retrieval, permeabilization
    • Secondary antibody conditions (diluent/dilution, incubation time/temperature)
    • Wash steps
    IP
    • Amount of protein used
    • Detection method
    • Matrix used for pull-down
    • Primary antibody conditions (diluent/dilution, incubation time/temperature)
    • Wash steps
    • Western blot conditions
    WB
    • Amount of protein loaded
    • Blocking conditions
    • Detection method
    • Electrophoresis and transfer conditions
    • Primary antibody conditions (diluent/dilution, incubation time/temperature)
    • Secondary antibody conditions (diluent/dilution, incubation time/temperature)
    • Wash steps
    Other
    • Blocking conditions, if applicable
    • Description of the experiment you are running, with assay conditions (protocol summary, concentrations, incubation conditions)
    • Detection method
    • Primary antibody conditions (diluent/dilution, incubation time/temperature)
    • Sample preparation (amount of protein /cell number /fixation or permeabilization conditions)
    • Secondary antibody conditions (diluent/dilution, incubation time/temperature)
  16. What are your areas of interest? (check all that apply) *







  17. *

  18. Which of these best describes your interest in RabMAbs?










  19. *



  20. *
  21. Testing procedure









  22. e.g. hsa-miR-145-5p

    Check miRNA names against mirBase entries

    This will help us to match your request against our miRNA database.

    This step is optional.

    Multiple entries in miRBase were detected for the following target(s), please confirm your selection below.

    miRNA Sequence Accession Reads Action
    0 validated miRNA

    The following targets were not recognised on miRBase, or too many possible matches were returned.

      Please correct these in the box above then select 'Check miRNA', or complete the form and a member of our team will be in touch.

      Error


    • e.g. let-7d-5p, let-7g-5p, let-7i-5p, miR-29b-3p

      Multiple entries in miRBase were detected for the following target(s), please confirm your selection below.

      miRNA Sequence Accession Reads Action
      0 validated Normalizer

      The following targets were not recognised on miRBase, or too many possible matches were returned.

        Please correct these in the box above then select 'Check normalizers', or complete the form and a member of our team will be in touch.

        Error


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