I want to use H2O2 as an inducer of apoptosis. How to prepare 1M H2O2 using
30% hydrogen peroxide?
Thank you all!
Lao WANG
> I want to use H2O2 as an inducer of apoptosis. How to prepare 1M H2O2 using
> 30% hydrogen peroxide?
The molecular weight of H2O2 is 34 daltons (or close enough to 34).
1M H2O2 = 34 g/L
30% H2O2 = 300 g/L
Do the math, and dilute it in ddH2O.
AC
--
Email: echo 36434455860060025978157675027927670979097959886449930P | dc
30% H2O2 is 300g/Liter
1M H2O2 is 34g/Liter (approx)
Will that suffice?
(This is what most of us are amazed about! Apoptosis is a good thing ---
thank God!)
> Hello!
>
> I want to use H2O2 as an inducer of apoptosis. How to prepare 1M H2O2
> using
> 30% hydrogen peroxide?
>
> Thank you all!
>
> Lao WANG
> _______________________________________________
> Methods mailing list
> Met...@net.bio.net
> http://www.bio.net/biomail/listinfo/methods
>
--
Hiranya S. Roychowdhury, Ph.D.
Asst. Professor,
Health & Public Services
Dona Ana Community College
New Mexico State University
Las Cruces, NM 88003
> In <mailman.479.12020...@net.bio.net>,
> WANG XF <wxf...@gmail.com> wrote:
>
>> I want to use H2O2 as an inducer of apoptosis. How to prepare 1M H2O2
>> using 30% hydrogen peroxide?
>
> The molecular weight of H2O2 is 34 daltons (or close enough to 34).
> 1M H2O2 = 34 g/L
> 30% H2O2 = 300 g/L
>
> Do the math, and dilute it in ddH2O.
>
> AC
Don't mouth-pipet the 30%.
3 % is OK, but don't overdo it - it tastes bad.
<grin>
--
Best regards
Han
email address is invalid
LOL! ... sorry I could'nt help but notice your last remark about
apoptosis....
Pow
> Hello!
> >
> > I want to use H2O2 as an inducer of apoptosis. How to prepare 1M H2O2
> > using
> > 30% hydrogen peroxide?
> >
------------------------------
>
> Message: 2
> Date: Mon, 4 Feb 2008 11:29:15 +0800
> From: "WANG XF" <wxf...@gmail.com>
> Subject: How to prepare 1M H2O2 using 30% hydrogen peroxide?
> To: met...@magpie.bio.indiana.edu
> Message-ID:
> <404daa2f0802031929ne6...@mail.gmail.com>
> Content-Type: text/plain; charset=ISO-8859-1
>
> Hello!
>
> I want to use H2O2 as an inducer of apoptosis. How to prepare 1M H2O2
> using
> 30% hydrogen peroxide?
>
> Thank you all!
>
> Lao WANG
>
>
> ------------------------------
>
> Message: 3
> Date: Mon, 04 Feb 2008 15:49:22 +1100
> From: Bean Long <ben....@yourfinger.anu.edu.au>
> Subject: Re: How to prepare 1M H2O2 using 30% hydrogen peroxide?
> To: met...@net.bio.net
> Message-ID: <47a69952$1...@clarion.carno.net.au>
> Content-Type: text/plain; charset=ISO-8859-1; format=flowed
>
> WANG XF wrote:
> > Hello!
> >
> > I want to use H2O2 as an inducer of apoptosis. How to prepare 1M H2O2
> using
> > 30% hydrogen peroxide?
> >
> > Thank you all!
> >
> > Lao WANG
>
> Here's a handy little link:
>
> http://www.trimen.pl/witek/calculators/stezenia.html
>
>
> ------------------------------
>
> Message: 4
> Date: Mon, 04 Feb 2008 12:38:46 GMT
> From: Aawara Chowdhury <aaw...@pontiff-playground.org>
> Subject: Re: How to prepare 1M H2O2 using 30% hydrogen peroxide?
> To: met...@net.bio.net
> Message-ID: <qHDpj.14164$M24....@newsfe17.lga>
>
> In <mailman.479.12020...@net.bio.net>,
> WANG XF <wxf...@gmail.com> wrote:
>
> > I want to use H2O2 as an inducer of apoptosis. How to prepare 1M H2O2
> using
> > 30% hydrogen peroxide?
>
> The molecular weight of H2O2 is 34 daltons (or close enough to 34).
> 1M H2O2 = 34 g/L
> 30% H2O2 = 300 g/L
>
> Do the math, and dilute it in ddH2O.
>
> AC
> --
> Email: echo 36434455860060025978157675027927670979097959886449930P | dc
>
>
> ------------------------------
>
> _______________________________________________
> Methods mailing list
> Met...@net.bio.net
> http://www.bio.net/biomail/listinfo/methods
>
> End of Methods Digest, Vol 33, Issue 3
> **************************************
>
that's the real issue. All your assumptions may be true.
IMHO is is *absolutely* necessary to specify m/v (mass/volume), m/m or
v/v. It even makes a difference if you (in this case rather
hypothetically as solid H2O2 does not exist [at least for a long
time]) mix 300 ml of H2O2 and 700ml of water, put 300 ml H2O2 in a
beaker and add water up to 1liter or vice versa. Does not make always
a real difference in the outcome of an experiment, but when you need
to troubleshoot a protocol or reproduce an experiment, this kind of
things will drive you nuts. There is nothing like a 'common sense' on
how to make procentual solutions. If possible, always state molar
contents, therefore.
All the best,
Wo
On 5 Feb., 15:45, "WANG XF" <wxfh...@gmail.com> wrote:
> *Thanks for your help!*
> **
> *30% H2O2 is 300g/L? or 300L/L or 300g/g?*
> **
> *Some of my colleagues have different suggestions.*
> **
> *Thank you!*
> **
> *Lao WANG*
> > **************************************
yes, that is true.... H2O2 would be w/w.... the MSDS generally does'nt give
the information, however, calling the company would give. Frankly, I did'nt
know that this is true for all industrial preparation..... Thank you Dima.
Pow
DK
On Feb 7, 2008 10:34 PM, <methods...@oat.bio.indiana.edu> wrote:
> Send Methods mailing list submissions to
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> Today's Topics:
>
> 1. R: buffer preparation (Prof. Piero Sestili)
> 2. Dulbecco`s PBS vs PBS pH7.4 (AS)
> 3. Re: How to prepare 1M H2O2 using 30% hydrogen peroxide?
> (Pow Joshi)
> 4. RE:Induction of apoptosis (Ozan Aygun)
> 5. Re: Dulbecco`s PBS vs PBS pH7.4 (DK)
>
>
> ----------------------------------------------------------------------
>
> Message: 1
> Date: Wed, 6 Feb 2008 16:02:26 +0100
> From: "Prof. Piero Sestili" <piero....@uniurb.it>
> Subject: R: buffer preparation
> To: <bertr...@gmail.com>, <met...@magpie.bio.indiana.edu>
> Message-ID: <002501c868d1$4d9d7f00$7d0c...@iram.it>
> Content-Type: text/plain; charset="iso-8859-1"
>
> First prepare a 2 M solution by diluting 2.26 ml of your stock to 10 ml,
> then make serial 1:10 dilutions down to 2 mM
> or
> prepare a 200 mM solution first diluting 226 ul of your stock to 10 ml
> and then another 1:100 dilution to 2 mM. As you prefer....
>
>
> Piero
>
>
> Prof. Piero Sestili
> Istituto di Farmacologia e Farmacognosia e
> Centro di Ricerca sull'Attività Motoria
> Università degli Studi di Urbino "Carlo Bo"
> Via "I Maggetti" 26
> 61029 URBINO (PU)
> Tel. 0722 303414; 0722 305524
> Fax 0722 303401
>
>
> -----Messaggio originale-----
> Da: methods...@oat.bio.indiana.edu
> [mailto:methods...@oat.bio.indiana.edu] Per conto di
> bertr...@gmail.com
> Inviato: mercoledì 6 febbraio 2008 12.11
> A: met...@magpie.bio.indiana.edu
> Oggetto: buffer preparation
>
> Hello,
>
> How do i work this out?
> :
>
> I need 2mM H2O2 from a stock solution H2O2 of 30%, density 1.11 gr/ml,
> M.W. 34
>
>
> anybody?
> thanks upfront
>
> b
> _______________________________________________
> Methods mailing list
> Met...@net.bio.net
> http://www.bio.net/biomail/listinfo/methods
>
>
>
>
> ------------------------------
>
> Message: 2
> Date: Wed, 6 Feb 2008 11:39:05 -0800 (PST)
> From: AS <Antonio...@gmail.com>
> Subject: Dulbecco`s PBS vs PBS pH7.4
> To: met...@net.bio.net
> Message-ID:
> <8dbed6dc-131a-4266...@e23g2000prf.googlegroups.com>
> Content-Type: text/plain; charset=ISO-8859-1
>
> What is the difference between Dulbecco`s PBS vs PBS pH7.4?
>
> Does it make a difference if I just use it to wash cells (293, MEFs
> etc) before trypsination or lysation?
>
> Thanks!
>
>
> ------------------------------
>
> Message: 3
> Date: Wed, 6 Feb 2008 13:09:45 -0500
> From: "Pow Joshi" <pow....@gmail.com>
> Subject: Re: How to prepare 1M H2O2 using 30% hydrogen peroxide?
> To: DK <d...@no.email.thankstospam.net>
> Cc: met...@magpie.bio.indiana.edu
> Message-ID:
> <710764ea0802061009j765...@mail.gmail.com>
> Content-Type: text/plain; charset=ISO-8859-1
> ------------------------------
>
> Message: 4
> Date: Wed, 6 Feb 2008 13:45:51 -0800 (PST)
> From: Ozan Aygun <metuge...@yahoo.com>
> Subject: RE:Induction of apoptosis
> To: met...@magpie.bio.indiana.edu
> Message-ID: <16475.9...@web90402.mail.mud.yahoo.com>
> Content-Type: text/plain; charset=iso-8859-1
>
> Hi,
>
> You may want to give try alpha-amanitin, which is a
> highly specific inhibitor of RNA polymerase II. It is
> known that exposure to this reagent causes apoptosis
> in human cells.
>
> Good luck,
>
> Ozan
>
>
>
> ____________________________________________________________________________________
> Looking for last minute shopping deals?
> Find them fast with Yahoo! Search.
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>
>
> ------------------------------
>
> Message: 5
> Date: Wed, 06 Feb 2008 22:25:02 GMT
> From: d...@no.email.thankstospam.net (DK)
> Subject: Re: Dulbecco`s PBS vs PBS pH7.4
> To: met...@net.bio.net
> Message-ID: <1tqqj.50$iB4...@newsfe07.lga>
>
> In article <
> 8dbed6dc-131a-4266...@e23g2000prf.googlegroups.com>, AS <
> Antonio...@gmail.com> wrote:
> >What is the difference between Dulbecco`s PBS vs PBS pH7.4?
>
> Probably none. Gibco used to specify its Dulbecco's PBS
> PH as 7.0-7.5. "PBS" is a mess. It can refer to a number of
> similar solutions, each with and without Ca2+ and/or Mg2+.
>
> >Does it make a difference if I just use it to wash cells (293, MEFs
> >etc) before trypsination or lysation?
>
> In the range in question, pH won't make a difference but for
> trypsinization there might be a diffrence between PBS
> containing divalents or not. Don't think it will be significant
> if you use trypsin-EDTA.
>
> DK
>
>
> ------------------------------
>
> _______________________________________________
> Methods mailing list
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>
> End of Methods Digest, Vol 33, Issue 6
> **************************************
>
--
Dr V K Gupta
Sr Microbiologist (Molecular Biology)
Insect Molecular Biology Lab
Department of Entomology
Punjab Agricultural University
Ludhiana (Pb)-141004- India
M: 09815963210