We fail if all we teach students is to be critical. We need to enable our students to conceive of a different and better way for things to be.

But in many cases these challenges are the result of your actions, the actions of others, social and political institutions, or a combination of all of these. Therefore, the first step in this kind of philosophical education is to shake students out of a complacent and uncritical acceptance of the world as it is.

it must also teach students to imagine how the world could be different than it is and, in so doing, to consider better ways for them and the world to be.

One answer to this question is pragmatic – philosophy teaches you to think and write logically and clearly. This, we tell our students, will be of use to them no matter what path they pursue. We advertise philosophy, then, as a broadly useful means to a variety of ends. There is a lot of truth to this dispassionate answer, but it is also rather disappointing. It sells philosophy short. A different sort of answer dives into profundity – philosophy aims to discover fundamental truths. Many disciplines aim at knowledge but philosophers, we solemnly tell our students, go deeper – we seek Knowledge with a capital K. This is undeniably the goal of many philosophers, but it can alienate some students (in particular, those who are not interested in pursuing an academic career). Why, these students might ask, is the knowledge that philosophy aims at any deeper than that of more practical fields such as medicine, science, or the law? And why should they care about this kind of knowledge? Even if most professional philosophers aim at the deepest kind of knowledge, this does not show that it is a valuable enterprise for all students, especially for those who are already overcoming significant hurdles to attend university.

The GMLC invokes a Nudm_UECM_Get service operation towards the home UDM of the target UE to be located with the GPSI or SUPI of this UE.

The external location services client sends a request to the GMLC for a location for the target UE identified by an GPSI or an SUPI. The request may include the required QoS, UE unaware indication and Supported GAD shapes. If location is required for more than one UE, the steps following below may be repeated and in that case the GMLC shall verify whether the number of Target UEs in the LCS request is equal to or less than the Maximum Target UE Number of the LCS client. If Maximum Target UE Number is exceeded, the GMLC shall reject the LCS request, the step 2-10 are skipped, and then GMLC respond to the client with proper error cause in the step 11.

demilitarization and peace

heroic struggle for the globalization of liberal freedoms

military hegemony as moral hegemony

yellow peril

model minority

a permanently abjected enemy whose depravity eclipses and necessitates the domestic and international brutalities of the U.S. world order

emergence of the contemporary liberal republic in South Korea (itself the imperfect achievement of decades of protracted working-class struggle) is retroactively presented as proof of how the U.S. “saved” Korea

“just war.”

“forgotten war,”

narratives of the pandemic

paragon of technocratic governance, a liberal-democratic foil in villainizing narratives of China, and a stage for classic Orientalist bloviations on Eastern collectivity and automatism versus Western individualism and indomitability

Accuracy (recovery

Linearity

Recovery studies and quality control

LC-MS Analysis

HPLC Analysis

Extraction and Cleanup

Sampling point, Sample Size and Sample collection

Analysis of Imidacloprid residues in various food commodities and hazard index estimation

Test Material

Animals

Chemicals

Sucrosc, 'frizma base, PMSI:, EIYSA, Tween-40TM IPolyoxycthylene (20) sorbitol ~nonopalmitatej. Tween-20TM, Glycerol, a-n~ercaptoethanol (2-ME), 1)imethyl sulphoxide (DMSO), TEMED. Ammoniu~n persulphate (APS), sodium dodecyl sulfate (SIX). Brilliant Blue G, Coomassie Blue, OPD, N-cthylmaleimide (NEM). Bovine Serum Albumin (USA), azetidinc-2-carboxilic acid (Azt). I,-canavanine (L-can). phosphatidylclioline, pl~osphatidylserine, phosphatidylethanolamine. cycloheximidr, 1,-amino acids, 1)-amino acids, valinomycin, CCCP, PercollTM, I,-proline agarose, L-argir~ine agarose, n-octyl-p-D- glucopyranoside, dansylated amino acids and egg-phoshatidylclioli~le (Egg-PC) were purchased from Sigma Chemicals Co. (St. Louis, USA

Materials

Materials

Preparation of ZnO/Ag2Onanocomposites

Photography, evaluation and documentation

Procedurefor SDS-PAGE

Materialsrequired for SDS-PAGE

Effect of temperature on xylanase activity

Effect of pH on xylanase activity

Effect of various carbon sourceson xylanase activity

Assayof xylanase activity

Dinitrosalicylate reagent (DNS)(per liter)

Citrate phosphate buffer

Reagents

Xylanase activity

Harvesting of cultures

Enzyme production (EP) medium

Inoculum preparation

Sporulation medium used for Trichodermasp

Maintenance of Trichodermasp. culture

Sterilization

Materials for xylanase induction

Induction of xylanase from Trichodermasp

Evaluation of bioagents against the pathogen

Laboratory screening of antagonists against the test pa

Effect of pHon growth and sporulation of the bioagent

Effect of temperature on growth of bioagent

Effect of different media on growth of bioagentTrichoderma

Cultural characteristicsof bioagent Trichoderma

Mycelial characteristicsof pathogen

Identificationof bioagent

Isolation and purification of Trichoderma sp.

Isolation and purification of pathogen, Fusarium udum

Isolation, purification and morphological characterization of pathogen and bioagent

Symptomatology

Collection of the diseased materia

Sterilization of laminar air flow

Sterilization of media and distilled water

Sterilization of glasswares

Sterilization procedure

Source of chemicals

Experimental site

Gel documentation and image analysis

Screening for virulence genes in V. parahaemolyticusfrom Cochin estuary, shrimp farm and seafood

Statistical analysis

Detection of hemolytic activity

Production of caseinase

Production of phosphatase

Bacterial strains used

DNAisolation

Detection of virulence genes tdhand trhby multiplex

Detection of type III secretion system genes

Production of chitinase

Production of DNas

Production of gelatinase

Production of Lipase

Production of amylase

Bacterial strains used

Screening of Vibriostrains for extracellular enzymes

Plasmid curing experiment

Plasmid profiling of the drug resistant strains

Gel documentation and image analysis

Detection ofblaNDM-1gene

Detection of blaCTX-Mgene

Detection of blaTEMgene

DNA isolation

Detection of beta-lactam antibiotic resistancegenes

MAR indexing

Antibiotic sensitivity tes

Statistical analysis

Gel documentation and image analysis

Detection of toxR gene

Detection of tlhgene

Extraction of genomic DNA

Detection of V. parahaemolyticusspecies-specific gene

Isolation of V. parahaemolyticuson HiCrome Vibrio

Isolation and identification of V. parahaemolyticus

PCR amplification of 16S rRNA gene

DNA isolatio

Molecular confirmation of Vibrioby 16S rRNA gene se

Resistance to ampicillin

Citrate utilisation tes

Nitrate reduction test

Production of β-galactosidase (ortho-Nitrophenyl β-D-galactopyranoside (ONPG)) test

Urease production

Gelatinase production

Growth at different temperatures

Salt tolerance tes

Voges Proskauer (acetoin production) test

Indole production

Carbon source utilisation tes

Carbohydrate fermentation test

Amino acids utilisation test (Decarboxylase/dihydrol

Species level identification

Oxidative-Fermentative test

Oxidase test

Gram staining

Presumptive identification

Isolation of Vibriospecies from water and sediment of Cochin estuary

Sample collection

Analysis of hydrographical parameters

Description of sampling site

Molecular confirmation of Vibrioby 16S rRNA gene s

Resistance to ampicillin

Citrate utilisation tes

Nitrate reduction tes

Production of β-galactosidase (ortho-Nitrophenyl β-D-galactopyranoside (ONPG)) test

Urease productio

Gelatinase productio

Growth at different temperature

Salt tolerance tes

Voges Proskauer (acetoin production) tes

Indole production

Carbon source utilisation t

Carbohydrate fermentation tes

Amino acids utilisation test (Decarboxylase/dihydrola

Species level identification

Oxidative-Fermentative test

Oxidase tes

Gram staining

Presumptive identification

Isolation of Vibriospecies from water and sediment of Cochin estuary

Sample collection

Analysis of hydrographical parameters

Description of sampling site

Sterilization

Plasmids and bacterial strain

Seed collection of different crops

Glasswares, plasticwares and equipments

Source of chemicals

Statistical analysis

Post-challenge survival

Determination of antileishmanial antibody responses in hamster

RT - PCR

cDNA synthesis and amplification

Formaldehyde gel electrophoresis

RNA isolation

Quantification of mRNA cytokines and inducible NO synthase (iNOS) in hamsters by Real time-PCR

NO production

LTT assay

DTH

Immunological assays

Vaccination schedule and assessment of parasitic burden

2 Anim

Parasite

Preparation of media for bacterial cell culture

Cloning of gene in pTZ57R/T (T/A cloning) vecto

Elution of amplified gene from the Gel

PCR amplification

Genomic DNA isolatio

Cloning, expression and purification ofADH

Python Molecular Viewer

PubChem Compound Database Screening

2D QSAR

Cygwin

Molecular Docking

Inhibitors Dataset

Active site analysis

Receptor X-ray structure

Molecular Docking

Inhibitors Dataset

Receptor X-ray Structure

RNA Interference

Cell transfection

Secondary antibodies

Primary antibodies

Antibodies used in our study

Cell culture

General reagents and plastic wares

Medium and Serum

Animals