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picture1_Bill Format In Word 11945 | Form 2 Seq | Sample Submission


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File: Bill Format In Word 11945 | Form 2 Seq | Sample Submission
a national facility established in 1951 form 2 for sanger sequencing service please contact us for quotation before sending the samples please fill form sign print and submit hard copy ...

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                                                        A National facility established in 1951
                                                          FORM-2 
                                     FOR SANGER SEQUENCING SERVICE
                                      Please contact us for quotation before sending the samples
                              (Please fill form, sign, print and submit hard copy/scanned hard copy)
                               Type of sample– Pure Culture/cloned plasmid DNA/PCR product
                       Pure Culture Type — Bacteria/ Fungi/ Yeasts/ Cyanobacteria/Microalgae/ etc—
                       DNA type- Purified Plasmid DNA from a recombinant clone
                       PCR product type- Purified/Non-purified/cycle-sequenced—
                       Ready to load type: Cycle sequenced and purified sample in hidi formamide
        I] User’s information 
        Name of Principal 
        Investigator / Scientist
        Prof./Dr.
        Address for correspondence
        Address for invoice/bill
         (if different than above)
        Contact information            Tel, Mobile             Fax               Email
        (STD/ISD code)
        Researcher’s information
        (If different than PI)
        Number of cultures/samples 
        Sent as slant/plate/stab/broth
        Partial (500-600 bp) or 
        full length (1100-1200 bp)
        Gene to be sequenced
        (16S, ITS, 18S or other)
        Payment details                Total Amount-
        (Amount in DD/other mode 
        should match with quote        Bank details-
        given by us)
                                       DD Number-                                                           Dated-
        DD should be in the name of ‘Director, National Chemical Laboratory’, Payable at Pune. No cash/cheque please !!
                                                                         NCIM sequencing form updated 09.07.2020
         II] Sample information
         PCR Purification method (if applicable)-
         Please attach separate sheet for additional samples, if required. 
           Sr. No.         Sample/Culture           Gram’s nature          Medium and temp.         PCR product/plasmid
                            code (e.g. A1)           (for bacteria)                                      DNA (ng/ µl)
              1
              2
              3
              4
              5
              6
              7
              8
              9
             10
             11
         Instructions for preparing PCR/plasmid:
         Provide template and/or primers in dissolved in PCR grade water. 
         Do not use EDTA based buffers; it may strongly inhibit sequencing reaction. 
         Provide samples in 0.2ml/ thin walled tubes.
         Use parafilm to tighten the sample tubes or culture plates. 
         Instructions for sending pure cultures:
         Contaminated culture plates/slants will not be accepted. They need to be pure and possibly well isolated.
         III] Template Information: Choose from following.
         Purified cloned plasmid DNA (provide 15µl of sample at 75-100 ng/µl)
         For recombinant Plasmid DNA- please provide 10 µl primers (10 picomple/µl concentration)
         Purified PCR product (provide 20 µl of sample at 30-40ng/µl)
         ss -Single stranded M13/phagemid DNA/ (provide 20µl of purified sample at 30-50 ng/µl)
         Please limit labels on tube to a max.5 characters.
         Enclose a gel picture for quantification and product quality. (OPTIONAL)
                                                                               NCIM sequencing form updated 09.07.2020
                                               Undertaking/Agreement
       I/We understood the norms and hence undertake to abide by the sample preparation guidelines. I/We submit the 
       sample(s) in good faith and NCIM will not be held responsible for loss/damage due to reason(s) beyond its control. 
       Signature of Researcher (with date)                     Signature of Principal investigator/Guide, Head
                                                                                   (Date, seal/stamp)
                                           FOR NCIM OFFICE USE ONLY
       Received by-                              Received on-
       Processed by -                            Approved by-
       Results sent on-
       Remarks, if any-
       Note: If PCR product is provided, the failed samples would be re-run only one time free of cost. 
       Fresh submission of same PCR product will be considered new submission and hence will be charged. 
       Use chromas lite and similar softwares to open .seq files. Can be freely downloaded from internet. Kindly note 
       that results are usually provided to the user in minimum 3-4 working weeks or earlier depending upon number 
       of samples given to us. Users can contact us by email if they do not hear from us within this time.
       Imp. Note-Cultures or sequencing samples should reach at NCIM-NCL by speed post or tracking based 
       overnight shipment; no acknowledgement will be given to end-user. Damaged/contaminated samples need to be
       submitted again as informed by us.
       For more information; visit NCIM webpage or email ncim@ncl.res.in or call at 020-25902670/2454. 
       Address: NCIM resource centre, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411008, 
       Maharashtra, India.
                                                                     NCIM sequencing form updated 09.07.2020
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...A national facility established in form for sanger sequencing service please contact us quotation before sending the samples fill sign print and submit hard copy scanned type of sample pure culture cloned plasmid dna pcr product bacteria fungi yeasts cyanobacteria microalgae etc purified from recombinant clone non cycle sequenced ready to load hidi formamide i user s information name principal investigator scientist prof dr address correspondence invoice bill if different than above tel mobile fax email std isd code researcher pi number cultures sent as slant plate stab broth partial bp or full length gene be its other payment details total amount dd mode should match with quote bank given by dated director chemical laboratory payable at pune no cash cheque ncim updated ii purification method applicable attach separate sheet additional required sr gram nature medium temp e g ng l instructions preparing provide template primers dissolved grade water do not use edta based buffers it may ...

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