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Goldfish

Goldfish (Carassius auratus) are a popular pet fish known for their vibrant colors and playful behavior.
These freshwater fish belong to the carp family and are closely related to common carp.
Goldfish are native to East Asia, but have been introduced worldwide as an ornamental species.
They thrive in a variety of aquatic environments, from small bowls to large ponds.
Goldfish are omnivorous, consuming a diet of plants, algae, and small invertebrates.
Their care and breeding have been well-studied, making them a valuable model organism for aquatic research.
Goldish are hardy and can live up to 20 years with proper housing and nutrition.
Researchers utilize golfish to study topics like behavior, genetics, and environmental toxicology.
PubCompare.ai can help locate the best protocols and products to enhance reproducibility in goldifsh research.

Most cited protocols related to «Goldfish»

Anopheles gambiae mosquitoes (G3 and Ngousso strains and their transgenic derivatives) were maintained at 28°C and 70-80% humidity in a 12/12 h day/night cycle. Anesthetized CD1 mice were used for blood feeding and larvae were fed finely ground Tetra Goldfish food (Tetra, Germany). The DSX transgenic strain, obtained in the G3 background, has been previously described [18 (link)].
The FK transgenesis plasmid was assembled by recombining three entry plasmids and one piggyBac destination plasmid using three-fragment Multisite Gateway cloning (Invitrogen) according to the manufacturer’s instructions. The resulting construct contained the attB1, attB2, attB3 and attB4 Gateway seam sites that delimit each of the three cassettes contributed by the entry plasmids (for the full annotated construct sequence refer to Additional file 1). The Vitellogenin (AGAP004203) promoter was amplified from A. gambiae genomic DNA using the following primers: 5’-TGACCTCGAGTTCAACTCGACC-3’ and 5’-GATATCGATGGTTCGGTTGTTCGCAGTTG-3’. The amplified fragment was cloned into Xho I and Cla I restriction sites of the YFP-containing entry vector. The AGAP002620 promoter region was amplified using primers: 5-CCGTCTAGACCGGGCTCTACAAAGTC-3’ and 5’-CAGCTCTCGAGCAGGAGGATCGTT-3’ and cloned as an Xba I - Xho I fragment into the tdTomato-containing entry vector. Embryos (n = 120) of the Ngousso strain were injected with a 200 ng/μl solution of the transgenesis plasmid and 20 surviving adults were back-crossed to Ngousso mosquitoes. A single transgenic mosquito male was recovered from the back-cross progeny. Further genetic crosses revealed that the transgene insertion was X-linked. The piggyBac insertion was mapped by inverse PCR as follows: 500 ng of genomic DNA were digested with Sau3AI or cocktails of blunt end restriction enzymes (ScaI HincII, DraI, SmaI PvuII, Fermentas), and re-ligated with T4 DNA ligase (Fermentas) in a final volume of 500 μl. The sample was ethanol-precipitated, re-suspended in 20 μl water, of which 2 μl were subjected to PCR. The piggyBac 5’ border of the insertion site was mapped by sequencing a product amplified with primers 5’-TGCACAGCGACGGATTCGCGCTATT-3’and 5’-AGGACATCTCAGTCGCCGCTTGGA-3’, followed by nested PCR with 5’-CGCGCTATTTAGAAAGAGAGAG-3’ and 5’-GAACTATAACGACCGCGTGAGTC-3’; or with 5’-GAACTATAACGACCGCGTGAGTC-3’ and 5’-CAGTGACACTTACCGCATTGACA-3’. The piggyBac 3’ border of the insertion site was mapped by sequencing the product amplified with primers 5’-CGAGGTTTATTTATTAATTTGAATAGATATTAAG-3’ and 5’-CGATATACAGACCGATAAAACACATGCGT-3’, followed by nested PCR with 5’-GCGTCAATTTTACGCATGATTATCTTT-3’ and 5’-ATTTACACTTACATACTAATAATAAATTCAAC-3’.
Amplified fragments were compared by BLAST to the Anopheles gambiae genome (VectorBase). The transposon insertion was mapped within a 232-base pair repeated element on the X chromosome. This short repeated element is broadly distributed in the genome, but at the position X: 22463464 is present in the Ngousso strain and absent from the G3 and PEST strains. The transgenic construct carried the EGFP gene under the control of a 3xP3 promoter [19 (link)] as a transgenesis selection marker, and two additional reporter genes: (i) YFPvenus[20 (link)] under the control of the A. gambiae Vitellogenin (AGAP004203) promoter and (ii) tdTomato[21 (link)] under the control of the AGAP002620 gene promoter [22 (link)]. The detailed characterization of these additional reporter constructs will be described elsewhere. Mosquitoes were reared and blood-fed on anesthetized mice in compliance with French and European laws on animal house procedures (agreement #E67-482-2 of the Direction of Veterinary services of the French Ministry of Agriculture).
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Publication 2012
Adult Animals Animals, Transgenic Anopheles gambiae Base Pairing BLOOD Cloning Vectors Crosses, Genetic Culicidae derivatives DNA Restriction Enzymes Embryo Ethanol Europeans Food Gene Expression Regulation Genes, Reporter Genome Goldfish HMN (Hereditary Motor Neuropathy) Proximal Type I Humidity Inverse PCR Jumping Genes Larva Males Mice, Laboratory Nested Polymerase Chain Reaction Oligonucleotide Primers Plague Plasmids Strains T4 DNA Ligase tdTomato Tetragonopterus Transgenes Vitellogenins X Chromosome
The starting point for this in silico analysis were the sequences for the two known salmon DNA transposons SALT1 [Genbank:L22865] [19 (link)] and Tss [Genbank:L12207] [18 (link)], as well as an analysis of the sequence of the T-cell receptor alpha locus of Salmo salar by RepeatMasker [46 ]. These two transposons as well as the RepeatMasker data were used to find faint similarities which were used in turn to find a larger number of each family in approximately 3 Mbp of sequence. The Dotter program [47 (link)] was used extensively to find regions of similar sequence, which were extracted and stored in an SQL database. The length of the transposon sequences was determined by identifying the inverted terminal repeat sequences where possible. Sequence alignments were performed with ClustalW [48 (link)] and phylogenetic trees generated with MEGA3.1 [49 (link)] using the Unweighted Pair Group Method with Arithmetic Mean (UPGMA), pairwise deletion, and a p-distance model. The entire alignment of the sequences was used in the phylogenetic reconstruction. Our salmon EST database was searched for the presence of sequences that are similar to the DNA transposon sequences that we found in salmon.
The following DNA sequences and BAC clones were used in this analysis. The Salmo salar TCRα locus [30 (link)], the major histocompatibility loci MHC class 1a and 1b [29 ], the growth hormone and interleukin loci (manuscripts in preparation), and zoneadhesin-like genes [Genbank:AY785950] and the Oncorhynchus mykiss sequences for the metallothionein gene [GENBANK:DQ156151], MHC1a [Genbank:AB162342] and MHC1b loci [Genbank:AB162343], and the IgH.A locus [Genbank:AY872256]. Genbank sequence entries were used in this study from a variety of other organisms (table 2): Oncorhynchus mykiss, Ictalurus punctatus, Esox lucius, Cyprinus carpio, Salvelinus namaycush, Salvelinus confluentus, Salvelinus fontinalis, Tanichthys albonus, Carassius auratus, Astatotilapia burtoni, Oryzias latipes, Petromyzon marinus, Danio rerio, Xenopus tropicalis, Xenopus laevis, Rana pipens, and Polypterus bichir. Sequences from Schistosoma japonicum EST Genbank data were found for transposon families as follows: DTSsa1 [Genbank:AY915112, AY809993], DTSsa2 [Genbank:AY816058, AY834394], DTSsa3 [Genbank:AY124772], DTSsa4 [Genbank:AY812589, AY915240], DTSsa5 [Genbank:AY813498], DTSsa6 [Genbank:AY813020], DTSsa7 [Genbank:AY813225, AY915121], SSTN1 [Genbank:AY809988, AY815476, AY915835], Tss [Genbank:AY915400, AY915891], and SALT1 [Genbank:AY223470, AY915102].
Representative sequences from all new families have been deposited in GenBank under accession numbers EF685954EF685960, EF685962EF685963, and EF685966EF685967.
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Publication 2007
Catfishes, Channel Clone Cells Cyprinus carpio Deletion Mutation DNA Transposons Esox lucius Genes Goldfish Growth Hormone Interleukins Inverted Terminal Repeat Jumping Genes Metallothionein Oncorhynchus mykiss Oryzias latipes Petromyzon marinus Rana Salmo salar Salvelinus Schistosoma japonicum Sequence Alignment Sequence Analysis Syncope T Cell Receptor alpha Chain Genes Xenopus laevis Zebrafish
The LRRs alignments within the TLR family were made for TLR1 from four species (human [Q15399, Q5FWG5, Q6FI64, Q32MK3], mouse [Q9EPQ1], pig [Q4LDR7, Q59HI9], Takifugu rubripes [Q5H727]); TLR2 from 17 species (human [O60603], mouse [Q9QUN7, Q8K3D9, Q811T5], pig [Q59HI8, Q5DX20, Q76L24], chicken [Q9DD78 (TLR2.1), Q9DGB6 (TLR2.2)], bovine [Q95LA9], rat [Q6YGU2], dog [Q689D1], rabbit [AAM50059], goat [ABI31733], horse [AAR08196], hamster [Q9R1F8], Cynomolgus monkey [Q95M53], domestic water buffalo [Q2PZH4], Nilgai [Q2V897], Takifugu rubripes [Q5H725], zebrafish [Q6TS42], Japanese flounder [Q76CT8]); TLR3 from 9 species (human [O15455, Q4VAL2, Q504W0], mouse [Q99MB1, Q3TM31, Q499F3], bovine [Q5TJ58, Q5TJ59], rat [Q7TNI8], buffalo [Q1G1A3], Rhesus macaque [Q3BBY1], Takifugu rubripes [Q5H721], zebrafish [Q6IWL5, Q32PW5], Japanese flounder [Q76CT7, Q76CT9]; TLR4 from 17 species (human [O00206, Q5VZI7, Q5VZI8, Q5VZI9], mouse [Q9QUK6, Q5RGT4, Q8K2T5], pig [Q68Y56, Q2TNK4, Q5F4K7, Q401C7], bovine [Q9GL65, Q6WCD5, Q8SQ55], rat [Q9QX05], hamster [Q9WV82], cat [P58727], lowland gorilla [Q8SPE8], horse [Q9MYW3], Pygmy chimpanzee [Q9TTN0], olive baboon [Q9TSP2], orangutan [Q8SPE9], Nilgai [Q2V898], American bison [Q3ZD70], dog [Q8SQH3], rabbit [AAM50060]; zebrafish [Q6NV08, Q6TS41(TLR4b)]; TLR5 from 8 species (human [O60602], pig [Q59HI7], mouse [Q9JLF7], bovine [Q2LDA0], chicken [Q4ZJ82], Japanese house mouse [Q1ZZX0], Takifugu rubripes [Q5H720, Q5H716(TLRS5)], rainbow trout [Q7ZT81]); TLR6 from 5 species (human [Q9Y2C9], mouse [Q9EPW9, Q7TPC5], rat [Q6P690], pig [Q59HI6, Q76L23], bovine [Q704V6, Q706D2]; TLR7 from 4 species (human [Q9NYK1], mouse [P58681, Q548J0], dog [Q2L4T3], Takifugu rubripes [Q5H719]); TLR8 from 4 species ((human [Q9NR97, Q495P4, Q495P6, Q495P7], mouse [P58682], pig [Q865R7], Takifugu rubripes [Q5H718]); TLR9 from 12 species (human [Q9NR96[, mouse [Q9EQU3], pig [Q5I2M3, Q865R8], bovine [Q5I2M5, Q866B2], dog [Q5I2M8], cat [Q5I2M7], Japanese flounder [Q2ABQ3], horse [Q2EEY0], sheep Q5I2M4], Ma's night monkey [Q56R09], Gilthead sea bream [Q3L273, Q3L274], Takifugu rubripes [Q5H717]]; TLR10 from two species (human [Q9BXR5, Q5FWG4, Q32MI7, Q32MI8], pig [Q4LDR6, Q59HI5]); TLR11 from mouse [Q6R5P0, Q32ME8]; TLR12 from mouse [Q6QNU9]; TLR13 from mouse [Q6R5N8]; TLR14 from Takifugu rubripes [Q5H726] and zebrafish [XP_687315]; TLR15 from chicken [ABB71177], TLR21 from Takifugu rubripes [NP_001027751], TLR22 from Takifugu rubripes [Q5H723], TLR23 from Takifugu rubripes [AAW70378], and TLR from rainbow trout [Q6KCC7, Q4LBC9], Atlantic salmon [Q2A132], goldfish [Q801F9]), Japanese lamprey [Q33E92, Q33E93] and green puffer (Fragment) [Q4S0D3]).
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Publication 2007
Bison Buffaloes Cattle Chickens Domestic Sheep Equus caballus Flounder Goat Goldfish Gorilla gorilla Hamsters Homo sapiens Japanese Lampreys Macaca fascicularis Macaca mulatta Mice, House Night Monkey Oncorhynchus mykiss Pan paniscus Papio anubis Pongo pygmaeus Pufferfish Rabbits Salmo salar Sparus aurata Takifugu rubripes TLR2 protein, human TLR5 protein, human TLR6 protein, human Water Buffalo Zebrafish
An observational study was conducted to validate the food atlas. Fifty college students from Nanjing Medical University, aged 20–22 years old, were invited to participate. The project was approved by the Human Research Ethics Committee of Nanjing Medical University (Protocol # 33; 2014/2015). Oral and written informed consent were obtained from each participant.
After selecting 10 types of food with Chinese characteristics, a meal was prepared according to the common processing and cooking methods. The investigators were responsible for weighing and calculating the raw food. The main ingredients included rice, tomato, celery, mushroom, rape (scientific name: Brassica napus L.; Chinese name: you cai; a green leafy vegetable), pork, crucian carp (scientific name: Carassius auratus; Chinese name: ji yu; one of the most common freshwater fish in China), egg, orange and banana. The investigators put the food in bowls or plates, and participants estimated the weight of the main ingredients. Then, the investigators put the bowl or plate containing the food on the background of vertical and horizontal coordinates calibrated in units of length (scale with 1 cm × 1 cm), next to the common objects known in daily life (a 355‐mL aluminum can and a piece of paper‐packed gum). The participants then estimated the weight of the main ingredients again according to the pictures of the relevant ingredients in the auxiliary reference food atlas. Each person estimated the weight of a food twice, with and without the use of the auxiliary reference food atlas. The differences between the estimated weight and the actual weight were then calculated and compared in the subsequent analysis of the data.
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Publication 2021
Agaricales Aluminum Apium graveolens var. dulce Banana Brassica napus Brassica rapa Carassius carassius Chinese Ethics Committees, Research Fishes Food Goldfish Homo sapiens Oryza sativa Plant Leaves Pork Raw Foods Students, Medical Tomatoes Vegetables
The three task- or set-switching tasks all required participants to switch back and forth between two subtasks. In each trial of the number–letter, participants saw a number-letter or letter-number pair in one quadrant of a box and categorized the number (2-9) as odd or even if the pair appeared in one of the top two quadrants, but categorized the letter (A, E, I, U, G, K, M, or R) as consonant or vowel if the pair appeared in one of the bottom two quadrants. In each trial of the color–shape task, participants saw a colored (red or green) shape (circle or triangle) and categorized the shape or color depending on a cue (C or S) that appeared above the stimulus. In each trial of the category-switch task, participants saw a word (alligator, bicycle, cloud, coat, goldfish, knob, lion, lizard, marble, mushroom, oak, pebble, shark, snowflake, sparrow, or table) and categorized it as describing something that is smaller or bigger than a soccer ball or living or nonliving, depending on a symbol (heart or crossed arrows) that appeared above the stimulus. In each trial (except for the number–letter single-task and predictable-switch blocks), the cue (darkening of the quadrant, letter, or symbol) started 350 ms before the target stimulus appeared. The cue and stimulus remained on the screen until the participant responded with one of two button presses (left indicated odd or consonant, red or circle, and small or nonliving, and right indicated even or vowel, green or triangle, and big or living), which triggered the next trial after a 350 ms response-to-cue interval. A 200 ms buzz sounded for errors.
Each task began with single-task blocks in which only one task was required (number then letter; color then shape; and animacy then size) for 24 trials each in the color–shape task and 32 trials each in the number–letter and category-switch tasks (block length differed slightly due to counterbalancing considerations). Each of these single-trial blocks was preceded by a 12-trial practice block and included two extra "warm-up" trials that were not analyzed. After these single-task blocks, participants completed two mixed blocks (56 trials each for color–shape, and 64 trials each for the other tasks), in which the two subtasks were pseudo-randomly mixed such that half the trials required switching subtasks. In the number–letter task they also completed two 64-trial predictable-switch blocks (not analyzed here) prior to the random mixed blocks, in which the stimuli circled the box in a clockwise pattern. The first of each type of switch block was preceded by a 24-trial practice block, and each switch block included four extra "warm-up" trials. The dependent measure for each task was the local switch cost: the difference between average RTs for switch trials and repeat trials in the random mixed blocks.
The primary change from the Wave 1 versions was the addition of the error signal (to further improve accuracy), the single-task blocks, the use of a 350-ms cue-to-stimulus interval throughout the mixed blocks, and the elimination of longer cue-to-stimulus interval blocks. In the Wave 1 version, participants completed four blocks that alternated between a 150 ms cue-to-stimulus interval and a 1,500 ms cue-to-stimulus interval (used to calculate residual switch costs); however, the blocks with the longer interval were not analyzed for the primary report (Friedman et al., 2008 (link)). The single-task blocks gave participants practice with the subtasks and response mappings and provided a baseline for calculating global switch costs and mixing costs (not analyzed here).
Publication 2015
Agaricales Alligators Goldfish Heart Lizards Marble Panthera leo Passeridae Sharks

Most recents protocols related to «Goldfish»

Deduced amino acid sequences of eomes genes were downloaded from the Ensembl genome browser (release 95, January 2019) for representative vertebrates, including human (Homo sapiens), mouse, chicken, and zebrafish. Sequence data of three other fishes were downloaded from species-specific genome databases, including grass carp (Ctenopharyngodon idella) (http://www.ncgr.ac.cn/grasscarp/), goldfish (https://research.nhgri.nih.gov/goldfish/), and common carp (http://www.fishbrowser.org/database/Commoncarp_genome/) (S2 Table).
Protein sequences of eomes gene from aforementioned species were aligned by ClustalW2 with default parameters [35 (link)]. A phylogenetic tree was built, using a JTT substitution model with maximum likelihood (ML) method with 1,000 bootstrap replications in MEGA6 software package [36 (link)].
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Publication 2023
Amino Acid Sequence Carps Chickens DNA Replication Fishes Gene Products, Protein Genes Genome Goldfish Grass Carp Homo sapiens Mice, House Vertebrates Zebrafish
Two copies of eomesa genes were identified in the genome of common carp. The eomesa1 and eomesa2 cDNA sequences of goldfish (Carassius auratus), Japanese silver crucian carp (Carassius auratus langsdorfii) and common carp downloaded from GenBank were used to identify and confirm the eomesa gene sequences and structures in the common carp genome (http://www.fishbrowser.org/database/Commoncarp_genome) using BLAST program (S1 Table).
The genomic sequences of common carp eomesa1 and eomesa2 were compared. Regions with low similarity and uniqueness to each gene were selected to design specific primer pairs to amplify eomesa1 and eomesa2 separately (Table 1, S1 Fig). The amplified fragments were then sequenced with the Sanger method. The sequencing results showed that these primers could be used to specifically amplify eomesa1 and eomesa2 of color common carp.
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Publication 2023
Carassius carassius Carps DNA, Complementary Genes Genome Goldfish Japanese Oligonucleotide Primers Silver
A BPA standard (purity > 98.0%), 2-methylimidazole (AR), and zinc nitrate hexahydrate (AR) were purchased from J&K Scientific Co., LTD (Beijing, China). Sodium hydroxide (AR), trisodium citrate dihydrate (99.0% purity), Na2CO3 (99.0% purity), anhydrous sodium sulfate (98.0% purity), and Polyvinyl pyrrolidone (Mw = 55,000, 99% purity) were purchased from Shanghai Aladdin Co., LTD (Shanghai, China). Methanol (AR), ethanol (AR), acetonitrile (AR), hydrochloric acid (AR), acetone (AR), ethyl acetate (AR), n-hexane (AR), and HNO₃ (AR) were purchased from Sinopharm Chemical Reagent Co., LTD (Shanghai, China). Potassium tetrachloroaurate (K(AuCl4), purity 97.0%) was purchased from Nanjing Senbeca Biotechnology Co., LTD (Nanjing, China). The above reagents, unless otherwise specified, are Analytical Reagents. The Crucian carp (Carassius auratus) fish was purchased from Jingdong (Shanghai, China).
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Publication 2023
2-methylimidazole Acetone acetonitrile Carassius carassius Ethanol ethyl acetate Fishes Goldfish Hydrochloric acid Methanol n-hexane Potassium Povidone Sodium Citrate Dihydrate Sodium Hydroxide sodium sulfate zinc nitrate hexahydrate
Live crucian carp (Carassius auratus) were purchased from Tongwei Sanlian Aquatic Products Trading Center (Chengdu, China), with weights of 230 ± 10 g and body lengths of 20 ± 2 cm. For all the experiments, intact, vigorous, and healthy crucian carp were used and cultured in polyethylene tank (0.5 × 0.4 × 0.3 m), with running water (20 ± 1 °C, pH 7.0 ± 0.5, the average dissolved oxygen was 6.0 mg/L), for 48 h before the experiments. According to the decision of the Animal Ethics Committee of Chengdu University, the fish used in experiments were washed with running water, dried with filter paper, and killed by knocking the head. Collect blood samples from the fish tail vein and the fish back muscle for biochemical analysis. Guanosine 5′-monophosphate disodium salt hydrate (5′-GMP-Na2, with purity 99.0%), cytidine 5′-monophosphate (5′-CMP, with purity 99.0%), uridine 5′-monophosphate disodium salt (5′-UMP-Na2, with purity 99.0%), 5′-inosinic acid disodium salt hydrate (5′-IMP-Na2, with purity 99.0%), and adenosine 5′-monophosphate disodium salt (5-AMP-Na2, with purity 99.0%) were purchased from Sigma-Aldrich (St. Louis, MO, USA); potassium dihydrogen phosphate, trichloroacetic acid, hydrochloric acid, and other chemical reagents were purchased from Chengdu Cologne Chemical Co., Ltd. (Chengdu, China); a lactate kit and glucose kit were purchased from Nanjing Jiancheng Bioengineering Institute (Nanjing, China).
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Publication 2023
Adenosine Monophosphate Animal Ethics Committees BLOOD Carassius carassius Cytidine Monophosphate Fishes Glucose Goldfish Guanosine Monophosphate Head Human Body Hydrochloric acid Inosine Monophosphate Lactates Muscle, Back Oxygen Polyethylene potassium phosphate, monobasic Sodium Chloride Tail Trichloroacetic Acid Veins
Goldfish Carassius auratus (body length 6.8 ± 0.8 cm; mass 12.4 ± 2.1 g), an experimental organism, were purchased from Choryang Aquarium (Busan, Republic of Korea) and acclimated for 7 days in six 300 L fresh water tanks in the laboratory. The fresh water was kept at 19.5 ± 1.1 °C and pH 7.8 with constant aeration. Feeding was stopped 24 h prior to the experiment.
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Publication 2023
Goldfish Human Body

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MS-222 is a chemical compound commonly used as a fish anesthetic in research and aquaculture settings. It is a white, crystalline powder that can be dissolved in water to create a sedative solution for fish. The primary function of MS-222 is to temporarily immobilize fish, allowing for safe handling, examination, or other procedures to be performed. This product is widely used in the scientific community to facilitate the study and care of various fish species.
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More about "Goldfish"

Goldfish (Carassius auratus) are a beloved aquatic pet known for their vibrant colors and captivating behavior.
These freshwater fish belong to the carp family and are closely related to the common carp.
Originating from East Asia, goldfish have been introduced globally as an ornamental species, thriving in a variety of aquatic environments, from small bowls to expansive ponds.
Goldfish are omnivorous, with a diverse diet that includes plants, algae, and small invertebrates.
Their care and breeding have been extensively studied, making them a valuable model organism for aquatic research.
These hardy fish can live up to 20 years with proper housing and nutrition.
Researchers leverage goldfish to explore a wide range of topics, such as behavior, genetics, and environmental toxicology.
Tools like the MS-222 anesthetic, TRIzol reagent for RNA extraction, and the NanoDrop 2000 spectrophotometer for nucleic acid quantification are commonly used in goldfish research.
Additionally, materials like fetal bovine serum (FBS), trypsin for cell dissociation, and collagenase for tissue digestion are integral to goldfish-related studies.
Experimental setups, such as the SZX16 stereomicroscope and the RM2245 rotary microtome, provide valuable insights into the anatomy and physiology of these fascinating creatures.
The HVL-IRM imaging system allows researchers to capture high-quality visual data, enhancing their understanding of goldfish biology and behavior.
PubCompare.ai is a powerful tool that can help researchers in the goldfish field locate the best protocols and products to ensure reproducibility and accuracy in their studies.
By comparing the latest literature, pre-prints, and patents, PubCompare.ai empowers scientists to stay at the forefront of goldfish research and make informed decisions about their experimental approaches.