Modern Blue Pills and Red Pills

Author(s):  
Asaf Algawi ◽  
Michael Kiperberg ◽  
Roee Shimon Leon ◽  
Amit Resh ◽  
Nezer Jacob Zaidenberg

This article presents the concept of blue pill, a stealth hypervisor-based rootkit, that was introduced by Joanna Rutkowska in 2006. The blue pill is a malicious thin hypervisor-based rootkit that takes control of the victim machine. Furthermore, as the blue pill does not run under the operating system context, the blue pill is very difficult to detect easily. The red pill is the competing concept (i.e., a forensics software that runs on the inspected machine and detects the existence of malicious hypervisor or blue pill). The concept of attestation of a host ensuring that no hypervisor is running was first introduced by Kennel and Jamieson in 2002. Modern advances in hypervisor technology and hardware-assisted virtualization enables more stealth and detection methods. This article presents all the recent innovation in stealth blue pills and forensics red pills.

Ransom ware is the most dangerous malware which locks the entire system data (files/folders) of user and demands ransom form user in order to decrypt data. Ransomware attacks are increasing day by day. Mobile phones are used not only for communication purpose but users also store their personal data and many other things in their mobile phone. 80% to 87% mobile phones are using Android operating system. Attackers have also targeted android smartphones just like personal computers. Due to rapid increase in ransomware we need to develop effective solution. There are different approaches like static, dynamic and hybrid which are used to detect ransomware.


Author(s):  
Anne F. Bushnell ◽  
Sarah Webster ◽  
Lynn S. Perlmutter

Apoptosis, or programmed cell death, is an important mechanism in development and in diverse disease states. The morphological characteristics of apoptosis were first identified using the electron microscope. Since then, DNA laddering on agarose gels was found to correlate well with apoptotic cell death in cultured cells of dissimilar origins. Recently numerous DNA nick end labeling methods have been developed in an attempt to visualize, at the light microscopic level, the apoptotic cells responsible for DNA laddering.The present studies were designed to compare various tissue processing techniques and staining methods to assess the occurrence of apoptosis in post mortem tissue from Alzheimer's diseased (AD) and control human brains by DNA nick end labeling methods. Three tissue preparation methods and two commercial DNA nick end labeling kits were evaluated: the Apoptag kit from Oncor and the Biotin-21 dUTP 3' end labeling kit from Clontech. The detection methods of the two kits differed in that the Oncor kit used digoxigenin dUTP and anti-digoxigenin-peroxidase and the Clontech used biotinylated dUTP and avidinperoxidase. Both used 3-3' diaminobenzidine (DAB) for final color development.


Author(s):  
E. Wisse ◽  
A. Geerts ◽  
R.B. De Zanger

The slowscan and TV signal of the Philips SEM 505 and the signal of a TV camera attached to a Leitz fluorescent microscope, were digitized by the data acquisition processor of a Masscomp 5520S computer, which is based on a 16.7 MHz 68020 CPU with 10 Mb RAM memory, a graphics processor with two frame buffers for images with 8 bit / 256 grey values, a high definition (HD) monitor (910 × 1150), two hard disks (70 and 663 Mb) and a 60 Mb tape drive. The system is equipped with Imaging Technology video digitizing boards: analog I/O, an ALU, and two memory mapped frame buffers for TV images of the IP 512 series. The Masscomp computer has an ethernet connection to other computers, such as a Vax PDP 11/785, and a Sun 368i with a 327 Mb hard disk and a SCSI interface to an Exabyte 2.3 Gb helical scan tape drive. The operating system for these computers is based on different versions of Unix, such as RTU 4.1 (including NFS) on the acquisition computer, bsd 4.3 for the Vax, and Sun OS 4.0.1 for the Sun (with NFS).


1974 ◽  
Author(s):  
Mark W. Stephens ◽  
Don Nelson ◽  
Gerald A. Hudgens

1988 ◽  
Vol 60 (02) ◽  
pp. 133-136 ◽  
Author(s):  
R Schneppenheim ◽  
H Plendl ◽  
U Budde

SummaryA luminescence assay was adapted for detection of von Willebrand factor multimers subsequent to SDS-agarose gel electrophoresis and electroblotting onto nitrocellulose. The method is as fast as chromogenic detection methods and appears to be as sensitive as autoradiography without the disadvantages of the latter.


2015 ◽  
Vol 14 (1) ◽  
pp. 282-288
Author(s):  
Israa Adnan Ibraheam Al-Baghdady ◽  
Ashwak Bassim Jassim ◽  
Zainab Khudher Ahmed

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