Tyrosine-protein kinase that acts as a cell-surface receptor for PDGFA, PDGFB and PDGFC and plays an essential role in the regulation of embryonic development, cell proliferation, survival and chemotaxis. Depending on the context, promotes or inhibits cell proliferation and cell migration. Plays an important role in the differentiation of bone marrow-derived mesenchymal stem cells. Required for normal skeleton development and cephalic closure during embryonic development. Required for normal development of the mucosa lining the gastrointestinal tract, and for recruitment of mesenchymal cells and normal development of intestinal villi. Plays a role in cell migration and chemotaxis in wound healing. Plays a role in platelet activation, secretion of agonists from platelet granules, and in thrombin-induced platelet aggregation. Binding of its cognate ligands - homodimeric PDGFA, homodimeric PDGFB, heterodimers formed by PDGFA and PDGFB or homodimeric PDGFC -leads to the activation of several signaling cascades; the response depends on the nature of the bound ligand and is modulated by the formation of heterodimers between PDGFRA and PDGFRB.
Anti-PDGFRα -http://www.stjohnslabs.com/pdgfra-antibody-2
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Essential for hedgehog signaling regulation: acts as both a negative and positive regulator of sonic hedgehog (Shh) and Indian hedgehog (Ihh) pathways, acting downstream of SMO, through both SUFU-dependent and -independent mechanisms . Involved in the regulation of microtubular dynamics. Required for proper organization of the ciliary tip and control of ciliary localization of SUFU-GLI2 complexes (By similarity). Required for localization of GLI3 to cilia in response to Shh. Negatively regulates Shh signaling by preventing inappropriate activation of the transcriptional activator GLI2 in the absence of ligand. Positively regulates Shh signaling by preventing the processing of the transcription factor GLI3 into its repressor form. In keratinocytes, promotes the dissociation of SUFU-GLI2 complexes, GLI2 nuclear translocation and Shh signaling activation.
Anti-Kif 7 -http://www.stjohnslabs.com/kif-7-antibody-p-98600
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Multifunctional transcription factor in ER stress response. Plays an essential role in the response to a wide variety of cell stresses and induces cell cycle arrest and apoptosis in response to ER stress. Plays a dual role both as an inhibitor of CCAAT/enhancer-binding protein (C/EBP) function and as an activator of other genes. Acts as a dominant-negative regulator of C/EBP-induced transcription: dimerizes with members of the C/EBP family, impairs their association with C/EBP binding sites in the promoter regions, and inhibits the expression of C/EBP regulated genes. Positively regulates the transcription of TRIB3, IL6, IL8, IL23, TNFRSF10B/DR5, PPP1R15A/GADD34, BBC3/PUMA, BCL2L11/BIM and ERO1L.
Anti-CHOP -http://www.stjohnslabs.com/chop-antibody-2
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
The protein encoded by this gene was originally identified as an ovarian tumor antigen monitored in ovarian cancer. The encoded protein contains a B-box/coiled coil motif, which is present in many genes with transformation potential. This gene is located on a region of chromosome 17q21.1 that is in close proximity to tumor suppressor gene BRCA1. Three alternatively spliced variants encoding the same protein have been identified for this gene.[4] One implied function lies in autophagy, where it acts a cargo receptor in selective autophagy.
Anti-NBR1 - http://www.stjohnslabs.com/anti-nbr1-antibody?filter_name=STJ98902
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Key regulator of mitochondrial calcium uniporter (MCU) required to increase calcium uptake by MCU when cytoplasmic calcium is high. MICU1 and MICU2 form a disulfide-linked heterodimer that stimulate and inhibit MCU activity, respectively. MICU1 acts as a stimulator of MCU that senses calcium level via its EF-hand domains: enhances MCU opening at high Ca2+ concentration, allowing a rapid response of mitochondria to Ca2+ signals generated in the cytoplasm. Regulates glucose-dependent insulin secretion in pancreatic beta-cells by regulating mitochondrial calcium uptake. Induces T-helper 1-mediated autoreactivity, which is accompanied by the release of IFNG.
Anti-MICU1 -http://www.stjohnslabs.com/micu1-antibody
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Serine/threonine kinase which acts as an essential component of the MAP kinase signal transduction pathway. MAPK1/ERK2 and MAPK3/ERK1 are the 2 MAPKs which play an important role in the MAPK/ERK cascade. They participate also in a signaling cascade initiated by activated KIT and KITLG/SCF. Depending on the cellular context, the MAPK/ERK cascade mediates diverse biological functions such as cell growth, adhesion, survival and differentiation through the regulation of transcription, translation, cytoskeletal rearrangements. The MAPK/ERK cascade plays also a role in initiation and regulation of meiosis, mitosis, and postmitotic functions in differentiated cells by phosphorylating a number of transcription factors. About 160 substrates have already been discovered for ERKs.
Anti-ERK1 -http://www.stjohnslabs.com/erk1-antibody-3
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
CD5 is a cluster of differentiation expressed on the surface of T cells (various species) and in a subset of murine B cells known as B-1a. The expression of this receptor in human B cells has been a controversial topic and up to date there is no consensus regarding the role of this receptor as a marker of human B cells. B-1 cells have limited diversity of their B-cell receptor due to their lack of the enzyme terminal deoxynucleotidyl transferase (TdT) and are potentially self-reactive. CD5 serves to mitigate activating signals from the BCR so that the B-1 cells can only be activated by very strong stimuli (such as bacterial proteins) and not by normal tissue proteins. CD5 was used as a T-cell marker until monoclonal antibodies against CD3 were developed.
Anti-CD5 -http://www.stjohnslabs.com/cd5-antibody-p-98608
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Tyrosine-protein kinase that acts as a cell-surface receptor for PDGFA, PDGFB and PDGFC and plays an essential role in the regulation of embryonic development, cell proliferation, survival and chemotaxis. Depending on the context, promotes or inhibits cell proliferation and cell migration. Plays an important role in the differentiation of bone marrow-derived mesenchymal stem cells. Required for normal skeleton development and cephalic closure during embryonic development. Required for normal development of the mucosa lining the gastrointestinal tract, and for recruitment of mesenchymal cells and normal development of intestinal villi. Plays a role in cell migration and chemotaxis in wound healing. Plays a role in platelet activation, secretion of agonists from platelet granules, and in thrombin-induced platelet aggregation. Binding of its cognate ligands - homodimeric PDGFA, homodimeric PDGFB, heterodimers formed by PDGFA and PDGFB or homodimeric PDGFC -leads to the activation of several signaling cascades; the response depends on the nature of the bound ligand and is modulated by the formation of heterodimers between PDGFRA and PDGFRB.
Anti-PDGFRα -http://www.stjohnslabs.com/pdgfra-antibody-2
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Essential for hedgehog signaling regulation: acts as both a negative and positive regulator of sonic hedgehog (Shh) and Indian hedgehog (Ihh) pathways, acting downstream of SMO, through both SUFU-dependent and -independent mechanisms . Involved in the regulation of microtubular dynamics. Required for proper organization of the ciliary tip and control of ciliary localization of SUFU-GLI2 complexes (By similarity). Required for localization of GLI3 to cilia in response to Shh. Negatively regulates Shh signaling by preventing inappropriate activation of the transcriptional activator GLI2 in the absence of ligand. Positively regulates Shh signaling by preventing the processing of the transcription factor GLI3 into its repressor form. In keratinocytes, promotes the dissociation of SUFU-GLI2 complexes, GLI2 nuclear translocation and Shh signaling activation.
Anti-Kif 7 -http://www.stjohnslabs.com/kif-7-antibody-p-98600
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Multifunctional transcription factor in ER stress response. Plays an essential role in the response to a wide variety of cell stresses and induces cell cycle arrest and apoptosis in response to ER stress. Plays a dual role both as an inhibitor of CCAAT/enhancer-binding protein (C/EBP) function and as an activator of other genes. Acts as a dominant-negative regulator of C/EBP-induced transcription: dimerizes with members of the C/EBP family, impairs their association with C/EBP binding sites in the promoter regions, and inhibits the expression of C/EBP regulated genes. Positively regulates the transcription of TRIB3, IL6, IL8, IL23, TNFRSF10B/DR5, PPP1R15A/GADD34, BBC3/PUMA, BCL2L11/BIM and ERO1L.
Anti-CHOP -http://www.stjohnslabs.com/chop-antibody-2
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
The protein encoded by this gene was originally identified as an ovarian tumor antigen monitored in ovarian cancer. The encoded protein contains a B-box/coiled coil motif, which is present in many genes with transformation potential. This gene is located on a region of chromosome 17q21.1 that is in close proximity to tumor suppressor gene BRCA1. Three alternatively spliced variants encoding the same protein have been identified for this gene.[4] One implied function lies in autophagy, where it acts a cargo receptor in selective autophagy.
Anti-NBR1 - http://www.stjohnslabs.com/anti-nbr1-antibody?filter_name=STJ98902
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Key regulator of mitochondrial calcium uniporter (MCU) required to increase calcium uptake by MCU when cytoplasmic calcium is high. MICU1 and MICU2 form a disulfide-linked heterodimer that stimulate and inhibit MCU activity, respectively. MICU1 acts as a stimulator of MCU that senses calcium level via its EF-hand domains: enhances MCU opening at high Ca2+ concentration, allowing a rapid response of mitochondria to Ca2+ signals generated in the cytoplasm. Regulates glucose-dependent insulin secretion in pancreatic beta-cells by regulating mitochondrial calcium uptake. Induces T-helper 1-mediated autoreactivity, which is accompanied by the release of IFNG.
Anti-MICU1 -http://www.stjohnslabs.com/micu1-antibody
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Serine/threonine kinase which acts as an essential component of the MAP kinase signal transduction pathway. MAPK1/ERK2 and MAPK3/ERK1 are the 2 MAPKs which play an important role in the MAPK/ERK cascade. They participate also in a signaling cascade initiated by activated KIT and KITLG/SCF. Depending on the cellular context, the MAPK/ERK cascade mediates diverse biological functions such as cell growth, adhesion, survival and differentiation through the regulation of transcription, translation, cytoskeletal rearrangements. The MAPK/ERK cascade plays also a role in initiation and regulation of meiosis, mitosis, and postmitotic functions in differentiated cells by phosphorylating a number of transcription factors. About 160 substrates have already been discovered for ERKs.
Anti-ERK1 -http://www.stjohnslabs.com/erk1-antibody-3
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
CD5 is a cluster of differentiation expressed on the surface of T cells (various species) and in a subset of murine B cells known as B-1a. The expression of this receptor in human B cells has been a controversial topic and up to date there is no consensus regarding the role of this receptor as a marker of human B cells. B-1 cells have limited diversity of their B-cell receptor due to their lack of the enzyme terminal deoxynucleotidyl transferase (TdT) and are potentially self-reactive. CD5 serves to mitigate activating signals from the BCR so that the B-1 cells can only be activated by very strong stimuli (such as bacterial proteins) and not by normal tissue proteins. CD5 was used as a T-cell marker until monoclonal antibodies against CD3 were developed.
Anti-CD5 -http://www.stjohnslabs.com/cd5-antibody-p-98608
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
This presentation mainly focuses on explanation about acid fast staining, their principle, reagents and procedure. And also about acid fast organisms. And a detailed explanation about the importance of Ziehl-neelson stain and errors occured during the procedure.
CD15 mediates phagocytosis and chemotaxis, found on neutrophils; expressed in patients with Hodgkin disease, some B-cell chronic lymphocytic leukemias, acute lymphoblastic leukemias, and most acute nonlymphocytic leukemias. It is also called Lewis x and SSEA-1 (stage-specific embryonic antigen 1) and represents a marker for murine pluripotent stem cells, in which it plays an important role in adhesion and migration of the cells in the preimplantation embryo. It is synthezised by FUT4 (fucosyltransferase 4) and FUT9.
Anti-CD15 -http://www.stjohnslabs.com/cd15-antibody-p-98642
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Physiology and Biochemistry-I (Marks-25)
a) Hematology
i) Study of compound microscope ii) Microscopically study of blood cells iii) Different types of WBC, erythrocytes and platelets iv) Examination of hemoglobin v) Differential count of WBC vi) Total count of RBC and WBC vii) Determination of clotting and bleeding time viii) Examination of clot under the microscope ix) Effect of chemical agents of RBC x) Fragility test of RBC. xi) Determination of erythrocytes sedimentation rate xii) Examination of haemin crystals
b) Histology: Histology of muscle, liver, spleen, stomach, duodenum, pancreas, lung, kidney, skin and endocrine glands.
c)Chemical physiology:
i) Qualitative test of carbohydrates, proteins and fats ii) Qualitative and quantitative experiments on digestive juice. iii) Examination of urine, estimation of main constituents and detection of abnormal constituents.
B. Pharm. (Honours) Part-IV Practical,Molecular biology & Biotechnology, MANIKImran Nur Manik
Molecular Biology & Biotechnology: (Marks –35)
a) Isolation of plasmid DNA
b) Estimation of DNA, RNA and oligonucleotides
c) Agarose-gel electrophoresis of nucleic acids
d) Determination of bacterial drug resistance by disk diffusion method.
e) Estimation of protein concentration by Lowry method
Bow-Tie cavity design for high power SHG green laser. A high power fiber laser at 1064nm is terminated into an external bow-tie cavity for efficient SHG generation at 532nm green.
Introducing a 2D (X-Y) Joystick controlled stage I designed and built for Optical Tweezers, but could be used with any inverted microscope. This was a low budget stage system composed of parts from different vendors.
I designed and built this stable, precise and very maneuverable 3D stage (controlled through Joystick) for any upright microscope configuration. The stage uses Physik Instrumente linear stage, piezo and a Logitech joystick.
I designed and built this near-field optical microscope- first version for Actoprobe LLC. The microscope is a combination of confocal and AFM. The measured resolution of the microscope is about 20nm. I will build more version of it in near future.
This is a new product of Actoprobe LLC: Scanning Laser Confocal Microscope. I designed and built the microscope to investigate the defects and laser burn patterns on the mirror and LBO crystal surfaces. The microscope can also be used for bio-imaging.
This presentation mainly focuses on explanation about acid fast staining, their principle, reagents and procedure. And also about acid fast organisms. And a detailed explanation about the importance of Ziehl-neelson stain and errors occured during the procedure.
CD15 mediates phagocytosis and chemotaxis, found on neutrophils; expressed in patients with Hodgkin disease, some B-cell chronic lymphocytic leukemias, acute lymphoblastic leukemias, and most acute nonlymphocytic leukemias. It is also called Lewis x and SSEA-1 (stage-specific embryonic antigen 1) and represents a marker for murine pluripotent stem cells, in which it plays an important role in adhesion and migration of the cells in the preimplantation embryo. It is synthezised by FUT4 (fucosyltransferase 4) and FUT9.
Anti-CD15 -http://www.stjohnslabs.com/cd15-antibody-p-98642
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Physiology and Biochemistry-I (Marks-25)
a) Hematology
i) Study of compound microscope ii) Microscopically study of blood cells iii) Different types of WBC, erythrocytes and platelets iv) Examination of hemoglobin v) Differential count of WBC vi) Total count of RBC and WBC vii) Determination of clotting and bleeding time viii) Examination of clot under the microscope ix) Effect of chemical agents of RBC x) Fragility test of RBC. xi) Determination of erythrocytes sedimentation rate xii) Examination of haemin crystals
b) Histology: Histology of muscle, liver, spleen, stomach, duodenum, pancreas, lung, kidney, skin and endocrine glands.
c)Chemical physiology:
i) Qualitative test of carbohydrates, proteins and fats ii) Qualitative and quantitative experiments on digestive juice. iii) Examination of urine, estimation of main constituents and detection of abnormal constituents.
B. Pharm. (Honours) Part-IV Practical,Molecular biology & Biotechnology, MANIKImran Nur Manik
Molecular Biology & Biotechnology: (Marks –35)
a) Isolation of plasmid DNA
b) Estimation of DNA, RNA and oligonucleotides
c) Agarose-gel electrophoresis of nucleic acids
d) Determination of bacterial drug resistance by disk diffusion method.
e) Estimation of protein concentration by Lowry method
Bow-Tie cavity design for high power SHG green laser. A high power fiber laser at 1064nm is terminated into an external bow-tie cavity for efficient SHG generation at 532nm green.
Introducing a 2D (X-Y) Joystick controlled stage I designed and built for Optical Tweezers, but could be used with any inverted microscope. This was a low budget stage system composed of parts from different vendors.
I designed and built this stable, precise and very maneuverable 3D stage (controlled through Joystick) for any upright microscope configuration. The stage uses Physik Instrumente linear stage, piezo and a Logitech joystick.
I designed and built this near-field optical microscope- first version for Actoprobe LLC. The microscope is a combination of confocal and AFM. The measured resolution of the microscope is about 20nm. I will build more version of it in near future.
This is a new product of Actoprobe LLC: Scanning Laser Confocal Microscope. I designed and built the microscope to investigate the defects and laser burn patterns on the mirror and LBO crystal surfaces. The microscope can also be used for bio-imaging.
An automated and user-friendly optical tweezers for biomolecular investigat...Dr. Pranav Rathi
An automated and user-friendly optical tweezers for biomolecular investigations; a versatile, automated, fast, precise and user friendly optical tweezers capable of doing verity of biomolecular experiments.
In one of the DNA-sequencing experiments based on change in pH difference due to release of proton per nuceotide added to DNA. There was considerable pH change in pH due to various factors out of which one was due to the pH-sensor position inside the well; sensor kept stable vs sensor moving in the well in circular motion gives different result. So the pH rocker is designed to simulate the hand motion for the sensor and stabilize the results.
http://openwetware.org/wiki/User:Pranav_Rathi/Notebook/OT/2012/05/21/pH-rocker_for_DNA-sequencing_experiments
Getting started with Arduino using LabView V9.
http://openwetware.org/wiki/User:Pranav_Rathi/Notebook/OT/2013/01/11/Getting_started_with_Arduino#LabView_Arduino_Interface_and_Firmware_installation
Extend your opto mechanical controls with lego for out of box control/servo c...Dr. Pranav Rathi
One can extend the mechanical controls on the opt-mechanical device with Lego and can also possibly servo control the impossible optics.
http://openwetware.org/wiki/User:Pranav_Rathi/Notebook/OT/2012/01/12/Extend_your_Opto-mechanical_controls_with_Lego_for_out_of_box_control#Design_and_construction
Slack (or Teams) Automation for Bonterra Impact Management (fka Social Soluti...Jeffrey Haguewood
Sidekick Solutions uses Bonterra Impact Management (fka Social Solutions Apricot) and automation solutions to integrate data for business workflows.
We believe integration and automation are essential to user experience and the promise of efficient work through technology. Automation is the critical ingredient to realizing that full vision. We develop integration products and services for Bonterra Case Management software to support the deployment of automations for a variety of use cases.
This video focuses on the notifications, alerts, and approval requests using Slack for Bonterra Impact Management. The solutions covered in this webinar can also be deployed for Microsoft Teams.
Interested in deploying notification automations for Bonterra Impact Management? Contact us at sales@sidekicksolutionsllc.com to discuss next steps.
Kubernetes & AI - Beauty and the Beast !?! @KCD Istanbul 2024Tobias Schneck
As AI technology is pushing into IT I was wondering myself, as an “infrastructure container kubernetes guy”, how get this fancy AI technology get managed from an infrastructure operational view? Is it possible to apply our lovely cloud native principals as well? What benefit’s both technologies could bring to each other?
Let me take this questions and provide you a short journey through existing deployment models and use cases for AI software. On practical examples, we discuss what cloud/on-premise strategy we may need for applying it to our own infrastructure to get it to work from an enterprise perspective. I want to give an overview about infrastructure requirements and technologies, what could be beneficial or limiting your AI use cases in an enterprise environment. An interactive Demo will give you some insides, what approaches I got already working for real.
Securing your Kubernetes cluster_ a step-by-step guide to success !KatiaHIMEUR1
Today, after several years of existence, an extremely active community and an ultra-dynamic ecosystem, Kubernetes has established itself as the de facto standard in container orchestration. Thanks to a wide range of managed services, it has never been so easy to set up a ready-to-use Kubernetes cluster.
However, this ease of use means that the subject of security in Kubernetes is often left for later, or even neglected. This exposes companies to significant risks.
In this talk, I'll show you step-by-step how to secure your Kubernetes cluster for greater peace of mind and reliability.
Epistemic Interaction - tuning interfaces to provide information for AI supportAlan Dix
Paper presented at SYNERGY workshop at AVI 2024, Genoa, Italy. 3rd June 2024
https://alandix.com/academic/papers/synergy2024-epistemic/
As machine learning integrates deeper into human-computer interactions, the concept of epistemic interaction emerges, aiming to refine these interactions to enhance system adaptability. This approach encourages minor, intentional adjustments in user behaviour to enrich the data available for system learning. This paper introduces epistemic interaction within the context of human-system communication, illustrating how deliberate interaction design can improve system understanding and adaptation. Through concrete examples, we demonstrate the potential of epistemic interaction to significantly advance human-computer interaction by leveraging intuitive human communication strategies to inform system design and functionality, offering a novel pathway for enriching user-system engagements.
State of ICS and IoT Cyber Threat Landscape Report 2024 previewPrayukth K V
The IoT and OT threat landscape report has been prepared by the Threat Research Team at Sectrio using data from Sectrio, cyber threat intelligence farming facilities spread across over 85 cities around the world. In addition, Sectrio also runs AI-based advanced threat and payload engagement facilities that serve as sinks to attract and engage sophisticated threat actors, and newer malware including new variants and latent threats that are at an earlier stage of development.
The latest edition of the OT/ICS and IoT security Threat Landscape Report 2024 also covers:
State of global ICS asset and network exposure
Sectoral targets and attacks as well as the cost of ransom
Global APT activity, AI usage, actor and tactic profiles, and implications
Rise in volumes of AI-powered cyberattacks
Major cyber events in 2024
Malware and malicious payload trends
Cyberattack types and targets
Vulnerability exploit attempts on CVEs
Attacks on counties – USA
Expansion of bot farms – how, where, and why
In-depth analysis of the cyber threat landscape across North America, South America, Europe, APAC, and the Middle East
Why are attacks on smart factories rising?
Cyber risk predictions
Axis of attacks – Europe
Systemic attacks in the Middle East
Download the full report from here:
https://sectrio.com/resources/ot-threat-landscape-reports/sectrio-releases-ot-ics-and-iot-security-threat-landscape-report-2024/
Elevating Tactical DDD Patterns Through Object CalisthenicsDorra BARTAGUIZ
After immersing yourself in the blue book and its red counterpart, attending DDD-focused conferences, and applying tactical patterns, you're left with a crucial question: How do I ensure my design is effective? Tactical patterns within Domain-Driven Design (DDD) serve as guiding principles for creating clear and manageable domain models. However, achieving success with these patterns requires additional guidance. Interestingly, we've observed that a set of constraints initially designed for training purposes remarkably aligns with effective pattern implementation, offering a more ‘mechanical’ approach. Let's explore together how Object Calisthenics can elevate the design of your tactical DDD patterns, offering concrete help for those venturing into DDD for the first time!
GraphRAG is All You need? LLM & Knowledge GraphGuy Korland
Guy Korland, CEO and Co-founder of FalkorDB, will review two articles on the integration of language models with knowledge graphs.
1. Unifying Large Language Models and Knowledge Graphs: A Roadmap.
https://arxiv.org/abs/2306.08302
2. Microsoft Research's GraphRAG paper and a review paper on various uses of knowledge graphs:
https://www.microsoft.com/en-us/research/blog/graphrag-unlocking-llm-discovery-on-narrative-private-data/
Encryption in Microsoft 365 - ExpertsLive Netherlands 2024Albert Hoitingh
In this session I delve into the encryption technology used in Microsoft 365 and Microsoft Purview. Including the concepts of Customer Key and Double Key Encryption.
14. PBS
Chemicals used in PBS: PBS and H2O or D2O
• Dissolve 1 table in
200mL of H2O or D2O
15. BGB
Blotting Grade Blocker
To make 5mg/ml BGB
solution in popping
buffer:
•First wiight out 15mg of
BGB poweder
•Add 1.5 ml of 1x pop
and mix by vortexing
•Run through .2μM
syringe filter using 3ml
syringe.
•Now store 5mg/ml BGB
in 1x pop buffer (minus
amount of protein that
stuck to filter) at 3C.
This should be good for
few weeks.