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(New page: '''Neutral Detergent Fiber''' '''Materials:''' *sodium sulfite (stored in chemical cabinets) *top-loading balance (2 decimal places) *spatula *alpha-amylase (stored in refrigerator) *5 mL...)
 
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'''Neutral Detergent Fiber'''
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'''Materials:'''
*sodium sulfite (stored in chemical cabinets)
*top-loading balance (2 decimal places)
*spatula
*alpha-amylase (stored in refrigerator)
*5 mL pipet
*neutral detergent solution (stored in room 113B)
*2000 mL flask
*acetone (in flammables cabinet below fume hood in room 113B)
*digestion apparatus (ANKOM fiber analyzer)
*analytical balance
*drying oven at 105oC
*dessicator
*zip-loc bags with dessicant pouches (recently recharged at 105oC)
*3 glass jars
*microwave
*hazardous waste container


'''Procedure'''


Close valve on ANKOM fiber analyzer.


Load filter bags into bag suspender, starting with bottom tray.  Place three bags per tray and stack trays on center post with each level rotated 120 degrees.  Insert bag suspender into fiber analyzer.


Weigh out 20 g sodium sulfite and add to fiber analyzer.
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Measure out approximately 2 L neutral detergent solution into flask (this may need to be done 2 x 1 L, due to foam)Add 4 mL alpha-amylase to solutionPour mixture into fiber analyzerPlace weight on bag suspender, turn on agitation and check liquid level.
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Close lid.  Heat to 100oC and agitate for 75 min.
==Overview==


After 60 min, fill 3 glass jars (to just below neck) with nanopure water.  Microwave 1st jar for 11 min.
Replace this sentence with a brief description of the protocol and its goal.


After 75 min, turn off heat and agitationOpen valve so solution drains into sink with cold water running.   
==Materials==
List reagents, supplies and equipment necessary to perform the protocol hereFor those materials which have their own OWW pages, link to that pageAlternatively, links to the suppliers' page on that material are also appropriate.


Open lid. Close valve. Add 4 mL alpha-amylase to heated rinse water.  Pour rinse into fiber analyzer.  Agitate for 5 minutes with lid open.  Microwave 2nd jar of nanopure water for 11 min.
*supply 1 (i.e. tubes of a certain size? spreaders?)
*reagent 1
*X &mu;L reagent 2
**component A (reagent 2 is made up of multiple components)
**component B
*equipment 1
*equipment 2


Repeat 2nd rinse with 4 mL alpha-amylase.
==Procedure==
#Step 1
#Step 2
#*Step 2 has some additional information that goes with it.  i.e. Keep at 4&deg;C.
#Step 3
##Step 3 has multiple sub-steps within it.
##Enumerate each of those.


For final (3rd) rinse, use hot water only.
==Notes==
Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input!
#List troubleshooting tips here. 
#You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
#Anecdotal observations that might be of use to others can also be posted here.


After final rinse is complete, remove bag suspender from fiber analyzer.  Gently squeeze bags (4-6 at a time) to remove excess water.
Please sign your name to your note by adding <font face="courier"><nowiki>'''*~~~~''':</nowiki></font> to the beginning of your tip.


Place bags in 1 L beaker.  Add acetone to cover (~400 mL) and let soak in fume hood for 3-5 min.  Gently squeeze bags (4-6 at a time) to remove acetoneLet air-dry on clean tray in fume hood for 1 h (until acetone has evaporated).  Pour used acetone into hazardous waste container.
==References==
'''Relevant papers and books'''
<!-- If this protocol has papers or books associated with it, list those references hereSee the [[OpenWetWare:Biblio]] page for more information. -->
<biblio>
#Goldbeter-PNAS-1981 pmid=6947258
#Jacob-JMB-1961 pmid=13718526
#Ptashne-Genetic-Switch isbn=0879697164
</biblio>


Place tray in 105oC oven to dry overnight.
==Contact==
*Who has experience with this protocol?


Remove bags from oven and place immediately in zip-loc bags (flatten to remove air) and into dessicatorAfter cool (~30 min), record NDF bag weight using appropriate analytical balanceProceed with ADF.
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Revision as of 13:00, 4 June 2009

This page is a template and should not be edited.
Click here, copy the source, and paste it into your page.



Interested in posting a protocol on OpenWetWare? Here is a template to help you do so.

Click the view source tab and copy everything below this line. Paste it into your new protocol page. Then replace the text in this page with your own protocol. Feel free to add or delete sections as appropriate.

Overview

Replace this sentence with a brief description of the protocol and its goal.

Materials

List reagents, supplies and equipment necessary to perform the protocol here. For those materials which have their own OWW pages, link to that page. Alternatively, links to the suppliers' page on that material are also appropriate.

  • supply 1 (i.e. tubes of a certain size? spreaders?)
  • reagent 1
  • X μL reagent 2
    • component A (reagent 2 is made up of multiple components)
    • component B
  • equipment 1
  • equipment 2

Procedure

  1. Step 1
  2. Step 2
    • Step 2 has some additional information that goes with it. i.e. Keep at 4°C.
  3. Step 3
    1. Step 3 has multiple sub-steps within it.
    2. Enumerate each of those.

Notes

Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input!

  1. List troubleshooting tips here.
  2. You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
  3. Anecdotal observations that might be of use to others can also be posted here.

Please sign your name to your note by adding '''*~~~~''': to the beginning of your tip.

References

Relevant papers and books

  1. Goldbeter A and Koshland DE Jr. An amplified sensitivity arising from covalent modification in biological systems. Proc Natl Acad Sci U S A. 1981 Nov;78(11):6840-4. DOI:10.1073/pnas.78.11.6840 | PubMed ID:6947258 | HubMed [Goldbeter-PNAS-1981]
  2. JACOB F and MONOD J. Genetic regulatory mechanisms in the synthesis of proteins. J Mol Biol. 1961 Jun;3:318-56. DOI:10.1016/s0022-2836(61)80072-7 | PubMed ID:13718526 | HubMed [Jacob-JMB-1961]
  3. ISBN:0879697164 [Ptashne-Genetic-Switch]

All Medline abstracts: PubMed | HubMed

Contact

  • Who has experience with this protocol?

or instead, discuss this protocol.