Whether acetic acid (acetate glacial) can be replaced with hydrochloride (HCl) to reduce pH?

More Muhammad Nur Hasan's questions See All

Why did my lead nitrate solution precipitate?

Previously, I made Pb(NO3) stock in miliQ water and diluted into buffer. But I tried different way yesterday. I prepared 100 uM of Pb(NO3) in buffer 10 mM TA containing 50 mM NaCl, pH: 7.0-7.4 The...

01 February 2020 1,521 2 View

How much degree Celcius for boiling HAuCl4 solution?

Yesterday I synthesized 13 nm colloidal gold nanoparticles using hotplate stirrer (T= 300 C, s= 600 rpm), the solution boiled for a long time (until bubles out). Even it had already ~ more than 1...

03 April 2019 524 6 View

Actually how many the limitations of TAE or TBE to use (re-use) in gel electrophoresis?

Normally, I have fresh prepared TAE/TBE buffer. But sometimes I see one of my colleagues who re-use it max. 3 times, Is it corret or not? Does it have any effect to the result? Thanks

02 March 2019 674 3 View

How to make disulfide from thiol?

I have DNA (disulfide modifier) has already become the Thiol due to adding TCEP. So I want to make it be disulfide again. Thanks

07 August 2018 318 0 View

What is good idea to block AuNPs surface?

I need to block AuNPs surface (space between Thiol DNA - AunNPs) to prevent binding interaction with streptavidin.

07 August 2018 6,595 2 View

How to solve precipitated PBS; 100 mM MgCl ?

Yesterday I prepared 100 mM of MgCl in PBS 1X then sterilized it by autoclave. But my buffer was precipitated. How to prevent this matter? Thanks

07 August 2018 3,736 0 View

How to calculate the amount of DNA strands for each goldnanoparticle?

I read one paper (Hai-Bo Wang, 2013/DOI: 10.1039/c3nj00328k), he claim that there are approximately 50 strands of DNA probe for each AuNP. But, when I check a table from this paper (please check...

06 July 2018 1,222 1 View

How much melting temperature and delta G are used by benchmarks to avoid DNA strand displacement?

I want to check the DNA strand displacement possibility of my DNA.

05 June 2018 531 0 View

Why the results of my marker (DNA Ladder 50 bp) bands turn to worse?

I use that DNA marker in same concentration of gel (10%) and running at 80 V for 80 minutes (everything is the same).

04 May 2018 7,935 8 View

How to move the DNA down that attached at the tube wall?

My DNA is sensitive with mechanical force such as vortex and spin-down machine. Thanks

04 May 2018 752 3 View

Enhanced Yellow Fluorescent Protein (Aequorea victoria) DNA sequence?

I am on the lookout for the Enhanced Yellow Fluorescent Protein (Aequorea victoria) DNA sequence. Does anyone know where I can find it? Thank you in advance

03 March 2021 3,568 1 View

Buffer to disrupt platelet alpha granules for PF4 quantification?

Hello! I want to quantify by ELISA the secreted (from platelets poor plasma) and the non-secreted (from platelet lysate) PF4 before and after TRAP stimulation. I will use the ELISA from R&D...

03 March 2021 1,499 2 View

Does the pressure(-600 mmHg) affects pH?

When I conducted the degassing experiment using decompression under anaerobic condition(and I used ferrous based chelating agent), the oxidized ferric were observerd. So, could you tell me the...

03 March 2021 4,892 5 View

Buffer Exchange using column packed with sephadex G-25 effect on protein concentration?

Hello, If i am doing a buffer exchange for an antibody of 1mg/mL, does the elution lose protein in the process of buffer exchange? For example, if i flow through 500 uL of 1mg/mL sample, and...

03 March 2021 6,299 3 View

What solvent can I used for Paal Knorr reaction between 6-amino hexanoic acid and 2.5 hexanedione?

I am try to make the Paal Knorr reaction between 2.5 hexnedione and 6-amino hexanoic acid, my problem is type of solvent to use, because 6-hexaminohexanoic acid is soluble in water but I am not...

02 March 2021 4,443 2 View

How optimize the Size Exclusion Chromatography?

Hello! I'll do a size exclusion chromatography, but I only have an open column, and I'll perform the peptide extraction from yeast, using buffer lysis (sodium phosphate 50 mM/NaCl 30 mM/DNAse and...

01 March 2021 2,215 2 View

Does anyone know HRM channel in a 2 plex QIAGEN Rotor- Gene Q qPCR can be used as a separate channel?

I am going to have 3 different probes in my qPCR work that I am going to do. But I realized that the machine we have in the lab is a Rotor-Gene Q 2plex HRM Platform, saying it has green, yellow,...

01 March 2021 8,544 1 View

Why are my bands weird in this Agarose gel?

Can someone please give me some possible things that could go wrong? Here is my recipe: 0.5g Agarose 50 mL of TAE 1x 1 uL ethyl bromide. Gel was run at 100V for 1 hour. The buffer used is also TAE.

01 March 2021 9,952 3 View

Which cell line should we use to perform biological dosimetry experiments?

We are preparing some experiments based on irradiating cells under different conditions in order to evaluate the effects in terms of DNA damage, genetic expression, etc. As our project is...

01 March 2021 3,355 3 View

What do I do with DLS peaks that are from the buffer?

I'm looking at the aggregation of my protein sample using DLS. Unfortunately, my buffer (20mM HEPES) also results in a set of peaks. These are at approximately 1 and 1000 d.nm. The lowest peak...

01 March 2021 9,015 2 View

Laurence Stuart Dawkins-Hall

No !!
You might obtain the right pH by using concentrated HCL but in effect you have added sodium chloride to a nascent solution of Tris acetate by using hydrochloric acid
You will need to make again

Katie A Burnette

You need to raise the pH from 7.4 to 8.2, not lower the pH. You'll have to add a base. Make sure your pH probe is properly calibrated, it seems very odd that your pH is lower than needed with a protocol that says to use glacial acid to adjust the pH.