eng genètica 3r

Yes or No

Played 1

Create copy

About this activity

biotec

Created by

Mariona Miquel Garcia

Spain

Download the paper version to play

Top 10 results

#	Player	Accuracy	time
1	Martina Xian Porcel Obiols October 20, 2025	% 73	09:08

Do you want to stay in the Top 10 of this game? Log in to identify yourself.

Make your own free game from our game creator

Compete against your friends to see who gets the best score in this game

Make challenge

Foot and Ankle Anatomy Quiz

Thilaxshi Suresh

United Kingdom

(9)

Test your knowledge of the bones, joints, and muscles of the foot and ankle with this interactive quiz. Answer with ✅ if the statement is correct and ❌ if it is incorrect.
Grammys for best song/record

Educaplay Educational Resources

Spain

(50)

Answer if these songs won the Grammy for Best Song or Record of the Year (the general ones, category Grammys do not count)
Is it created with Artificial Intelligence? - Complete game

Educaplay Educational Resources

Spain

(17)

Images, songs... Nothing is what it seems anymore. Are they generated with AI, or are they real?
Is it true?

Educaplay Educational Resources

Spain

(59)

Answer if the following sentences about general culture are true or not.
Adjective Checker

Erika Moreno

Ecuador

(14)

In this game, you will have to determine if the adjective provided accurately describes the noun. Test your knowledge of adjectives and see if you can spot the correct matches!

		%
	Anonymous	%
		%
		%

Print your game

eng genètica 3r


eng genètica 3rOnline version biotec by Mariona Miquel Garcia 1 Sticky-end ligation is more eûcient than blunt-end ligation Sí No 2 It is generally accepted that the optimal length of PCR product is between 18-22 bp Sí No 3 The gen called lacZ, encodes for beta-galactosidase, the enzyme involved in the breakdown of X-gal that give a deep blue colored product Sí No 4 Linkers are attached to the end of sticky DNA molecule and can be cut to generate blunt ends Sí No 5 Klenow fragment can generate a new strand of DNA from an RNA template Sí No 6 Cosmids are plasmids with an special module that permits the packaging of recombinant genomes into lambda particles Sí No 7 To sequence the entire genome of an organism the most appropriate method is the Sanger method Sí No 8 Genomic libraries are constructed using cDNA Sí No 9 RT-PCR allows you to compare gene expression between samples Sí No 10 The signal peptide that is often included when producing recombinant proteins in Piccia pastors has the role of targeting the recombinant protein to the micocondria where it can accumulate withot tox Sí No 11 In RNase protection assay you can only detect one RNA in each reaction Sí No 12 Inducible promoters allow the regulation of the expression of particular cDNAs placed under their control Sí No 13 RNA seq uses next-generation sequencing to quantify DNA in a sample at a precise moment in time Sí No 14 mRNA is easily puriûed from total RNA using oligodC aûnity columns Sí No 15 The substrate for DNA packaging in lambda particles ic circular DNA Sí No 16 Lambda can undertake the lysogenic cycle only when the genome is recombinant Sí No 17 The yeast two-hybrid system is very useful but it does not allow to identify protein-protein interactions Sí No 18 When designing a primer to introduce a change of amino acid in a protein, the mutation or mutations is/are in the center of the mutagenic primer Sí No 19 The quick-change mutagenesis kit relies in methylation of the sequence GATC in E.coli and the lack of such modiûcation in newly in vitro-synthesized DNA when using PCR Sí No 20 Microarrays can be used to answer this question: Sí No 21 Inducible promoters allow the regulation of the expression of particular cDNAs placed under their control Sí No 22 Haripins in primer loop are important for a correct binding to target DNA sequence Sí No 23 HIgher number of genes are detected in RNA seq versus Microarrays Sí No 24 Different restriction enzymes can generate the same sticky ends Sí No 25 In real time PCR a house keeping gene is used as an internal control Sí No 26 Northern blot could be used to detect expression of a speciûc gene in diûerent tissues Sí No 27 The hybridization probe for primer extension is a synthesized radio labeled oligonucleotide Sí No 28 Choosing the appropriate homology arms allows precise integration of DNA sequences in the yeast genome Sí No 29 Cell extracts used for in vitro translation provide ribosomes and tRNA Sí No 30 .The Gateway cloning technology is based on site-speciûc recombination system Sí No 31 In the Northern blot RNA is transferred from the electrophoresis agarose gel to the blotting nitrocellulose membrane Sí No 32 In Real Time PCR we always use ûuorescent reporters to follow ampliûcation process Sí No 33 An expression cassette consists on a promoter the coding sequences for a particular protein and a transcription termination signal Sí No 34 Multiplex-PCR uses one pair of primers annealing to diûerent target sequences Sí No 35 Asymmetric PCR uses excess of only one primer and preferentially ampliûes one strand of the target DNA Sí No 36 PCR can be used for analyzing genotype or mouse models Sí No 37 Depending on your goals or needs, cDNA libraries are prepared in diûerent vectors Sí No 38 In RACE PCR you can amplify a full length sequence of an RNA transcript Sí No 39 When working with lambda, replacement vectors accept less DNA than the insertion vectors Sí No 40 Housekeeping gene has diûerent expression in normal or pathological conditions Sí No 41 Polynucleotide kinase dephosphorilates 39-OH ends of DNA Sí No 42 When producing a new recombinant protein, independently of your goals, you must always add an aûnity tag Sí No 43 In situ hybridization allows you to locate a fragment of nucleic acid whitin a histologic section Sí No 44 The northern blot is a technique used to study ene expression by detection of DNA in a sample Sí No 45 Random priming is a good method to get speciûc labelling of one of the two DNA strands Sí No 46 Oligo(dT) primers are used for cDNA synthesis reactions because of their speciûcity for mRNA Sí No 47 All restriction endonucleases recognize hexanucleotide target sites and has a palindromic sequence Sí No 48 There exist several technological platforms for high-throughput sequencing. Depending on your needs one platform may be more appropriate than the other Sí No 49 In a PCR is always necessary to use degenerate primers Sí No 50 Phages derived from f1 that display a fusion protein in their surface cannot be generated so that they contain a genome with the DNA sequence that codes for that particular fusion protein Sí No 51 At 94oC, DNA denaturates and strands are separated Sí No 52 The Sanger method relies on the Watson and Crick base pairing Sí No 53 Polymerases requires a primer to synthese new DNA Sí No 54 To identify recombinant colonies, one strategy is to replica plated onto agar medium that contains a second antibiotic, for instance, tetracycline Sí No 55 Endonucleases removes nucleotides from the end of a DNA molecule Sí No 56 The product of lambda particles containing a cosmic genome requires the lysis of infected cells that contain such genome Sí No

eng genètica 3r

Yes or No

About this activity

Created by

Download the paper version to play

Top Games

Yes or No

Foot and Ankle Anatomy Quiz

Yes or No

Grammys for best song/record

Yes or No

Is it created with Artificial Intelligence? - Complete game

Yes or No

Is it true?

Yes or No

Adjective Checker

eng genètica 3rOnline version

by Mariona Miquel Garcia

Sticky-end ligation is more eûcient than blunt-end ligation

It is generally accepted that the optimal length of PCR product is between 18-22 bp

The gen called lacZ, encodes for beta-galactosidase, the enzyme involved in the breakdown of X-gal that give a deep blue colored product

Linkers are attached to the end of sticky DNA molecule and can be cut to generate blunt ends

Klenow fragment can generate a new strand of DNA from an RNA template

Cosmids are plasmids with an special module that permits the packaging of recombinant genomes into lambda particles

To sequence the entire genome of an organism the most appropriate method is the Sanger method

Genomic libraries are constructed using cDNA

RT-PCR allows you to compare gene expression between samples

The signal peptide that is often included when producing recombinant proteins in Piccia pastors has the role of targeting the recombinant protein to the micocondria where it can accumulate withot tox

In RNase protection assay you can only detect one RNA in each reaction

Inducible promoters allow the regulation of the expression of particular cDNAs placed under their control

RNA seq uses next-generation sequencing to quantify DNA in a sample at a precise moment in time

mRNA is easily puriûed from total RNA using oligodC aûnity columns

The substrate for DNA packaging in lambda particles ic circular DNA

Lambda can undertake the lysogenic cycle only when the genome is recombinant

The yeast two-hybrid system is very useful but it does not allow to identify protein-protein interactions

When designing a primer to introduce a change of amino acid in a protein, the mutation or mutations is/are in the center of the mutagenic primer

The quick-change mutagenesis kit relies in methylation of the sequence GATC in E.coli and the lack of such modiûcation in newly in vitro-synthesized DNA when using PCR

Microarrays can be used to answer this question:

Inducible promoters allow the regulation of the expression of particular cDNAs placed under their control

Haripins in primer loop are important for a correct binding to target DNA sequence

HIgher number of genes are detected in RNA seq versus Microarrays

Different restriction enzymes can generate the same sticky ends

In real time PCR a house keeping gene is used as an internal control

Northern blot could be used to detect expression of a speciûc gene in diûerent tissues

The hybridization probe for primer extension is a synthesized radio labeled oligonucleotide

Choosing the appropriate homology arms allows precise integration of DNA sequences in the yeast genome

Cell extracts used for in vitro translation provide ribosomes and tRNA

.The Gateway cloning technology is based on site-speciûc recombination system

In the Northern blot RNA is transferred from the electrophoresis agarose gel to the blotting nitrocellulose membrane

In Real Time PCR we always use ûuorescent reporters to follow ampliûcation process

An expression cassette consists on a promoter the coding sequences for a particular protein and a transcription termination signal

Multiplex-PCR uses one pair of primers annealing to diûerent target sequences

Asymmetric PCR uses excess of only one primer and preferentially ampliûes one strand of the target DNA

PCR can be used for analyzing genotype or mouse models

Depending on your goals or needs, cDNA libraries are prepared in diûerent vectors

In RACE PCR you can amplify a full length sequence of an RNA transcript

When working with lambda, replacement vectors accept less DNA than the insertion vectors

Housekeeping gene has diûerent expression in normal or pathological conditions

Polynucleotide kinase dephosphorilates 39-OH ends of DNA

When producing a new recombinant protein, independently of your goals, you must always add an aûnity tag

In situ hybridization allows you to locate a fragment of nucleic acid whitin a histologic section

The northern blot is a technique used to study ene expression by detection of DNA in a sample

Random priming is a good method to get speciûc labelling of one of the two DNA strands

Oligo(dT) primers are used for cDNA synthesis reactions because of their speciûcity for mRNA

All restriction endonucleases recognize hexanucleotide target sites and has a palindromic sequence

There exist several technological platforms for high-throughput sequencing. Depending on your needs one platform may be more appropriate than the other

In a PCR is always necessary to use degenerate primers

Phages derived from f1 that display a fusion protein in their surface cannot be generated so that they contain a genome with the DNA sequence that codes for that particular fusion protein

At 94oC, DNA denaturates and strands are separated

The Sanger method relies on the Watson and Crick base pairing

Polymerases requires a primer to synthese new DNA

To identify recombinant colonies, one strategy is to replica plated onto agar medium that contains a second antibiotic, for instance, tetracycline

Endonucleases removes nucleotides from the end of a DNA molecule

The product of lambda particles containing a cosmic genome requires the lysis of infected cells that contain such genome