12 Questions 16 Answers 0 Followers
Questions related from Syeda Mahreen Hassan
I want to use E. faecalis JH22 as competent cells to express my protein using anhydrotetracycline (ATc) to induce protein expression i need some standard protocol if someone has use it before.
07 July 2019 9,567 2 View
website,genome sequence
02 February 2019 7,218 2 View
As PET duet vector is for cloning of two gene of interest;i want the protocol for it.
07 July 2018 9,136 0 View
is my plasmid is contaminated with ethanol;how to avoid this contaminated
01 January 2018 4,344 0 View
I run gel electrophoresis to confirm digestion of my plasmid however my samples are remaining at the start of the gel. I have remade wash buffers and carrier buffers but am still not seeing my...
01 January 2018 6,293 0 View
can anyone please recomend me any primer
11 November 2017 606 1 View
in which i resuspend my pellet against which buffer i have to dialysis.
11 November 2017 5,630 2 View
Tx6119( M15 containing fragment of SwpA26-226 from TX82 cloned into pQE30),when i run it as control without injecting IPTG i never saw any band on SDS-gel.
10 October 2017 3,242 4 View
Can anyone suggest why i am not getting any bands
10 October 2017 5,733 3 View
TX6119- Fragments were cloned into the expressionvector pQE30 (Qiagen) and transformed into M15 (pREP4) cells(Qiagen).i want to make culture in LB broth to do miniprep i am confuse how much i add...
08 August 2017 378 4 View
Positive and negative control
06 June 2017 5,981 3 View
growing the bacteria(LB broth) for protein expression: the optical density(1.2) , is this good for protein expression(before IPTG).
04 April 2017 3,212 13 View