Chemicals

MIDSCI is Your Trusted Source for High-Quality Lab Chemicals and Reagents

Looking for reliable chemicals to power your research? MIDSCI delivers a full range of high-purity reagents, solvents, and buffers designed for life science, pharmaceutical, microbiology, and organic chemistry workflows. From essential acids and bases to specialized biochemicals, growth media, and DNA kits, our inventory ensures precision, consistency, and compliance, backed by Certificates of Analysis (COAs) and Safety Data Sheets (SDS).

Explore PR1MA Chemicals, our premium line of USP- and ACS-grade chemicals

Perfect for molecular biology, plant science, and cellular research, PR1MA products offer full traceability and documentation for your peace of mind.

Shop now for high-quality chemicals or contact our experts for personalized recommendations!

Looking for ways to save? Sign up for our newsletter to hear about upcoming offers!

|◀ 133 - 144 of 434 ▶|
View:

These items have been discontinued and will only be available while supplies last.
Need a great Reverse Transcriptase product at a great price? Try PR1MA!
 
 

Click here for PCR or here for qPCR to order.


Bullseye EasyScript Reverse Transcriptase

Application

  • Synthesis cDNA froma single-stranded RNA or DNA primer extension
  • Sequencing dsDNA
  • cDNA library
  • Template production for use in PCR
  • 3'-end labeling of duplex DNA via end-filling reactions

EasyScript Reverse Transcriptase is a genetically modified form of Moloney Murine Leukemia Virus Reverse Transcriptase (M-MLV). Both the EasyScript and EasyScript Plus are RNase H deficient (negative). The enzyme is purified from bacteria h o s t as a single holoenzyme of 71 kDa with the capacity of first-strand cDNA synthesis of template up to 9kb and can be used for routine cDNA synthesis.

Kit Components

ComponentsEasyScript Reverse Transcriptase
Item #G231G232
EasyScript RTase (200 U / uL)5,000 U20,000 U
5x RT buffer150 uL600 uL
Size25 rxns100 rxns

Storage Buffer
 
50 mM Tris-HCl (pH 8.3), 100 mM NaCl, 0.1 mM EDTA, 5 mM DTT, 0.1% (v/v) Triton X-100, and 50% (v/v) glycerol.

Storage
 
Store at -20°C in a frost-free freezer. Multiple freezing and thawing of RNA should be avoided. Keep RNA on ice all the time. It is recommended that the first strand cDNA synthesis is carried out under conditions where RNase contamination has been eliminated.

General Protocol

RT-PCR reactions should be assembled in a RNA-free environment. The use of "clean", automatic pipettes designated for PCR and aerosol resistant barrier tips are recommended.

1. Thaw template RNA and all reagents on ice. Mix each solution by vortexing, and centrifuge briefly to collect residual liquid from the sides of the tubes. 
2. Prepare the following reaction mixture in a PCR tube on ice:

 VolumeConcentration (final 20 uL)
Total RNA, or poly(A)+RNAVariable0.5-5µg per reaction
50ng-0.5 uG per reaction
Oligo(dT) (10 uM)1 uL0.5 uM
or Random Primer (10 uM)1 uL0.5 uM
or Sequence-specific PrimerVariable10-15 pM
dNTP (10mM)1 uL500 uM
5X RT Buffer4 uL1X
RNasin (40 U/ uL)0.5 uL20 U per reaction
EasyScript RTase (200 U/ uL)
1 uL200 U per reaction
RNase-free H2OVariable-
Final volume20 uL-

3. Incubate at 25°C for 10 minutes if random primer is used. Omit this step if Oligo(dT) primer or sequence specific primer are used.
4. Incubate the mixture at 42°C for 60 minutes.
5. Stop the reaction by heating at 85°C for 5 minutes. 
6. Chill on ice. The newly synthesized first-strand cDNA now can be used directly for PCR amplification.

Notes:
1. Isolation of poly(A)+ RNA from total RNA is not mandatory; however, doing so may improve the yield and purity of the final product. 
2. RNA sample must be free of contaminating genomic DNA.
3. Unlike the oligo(dT) priming, which usually requires no optimization, the ratio of a randomprimer to RNA is critical in terms of the average length of cDNA synthesized in the reaction. Increasing the ratio of random primer/RNA will result in higher yield of shorter (~500 bp) cDNA, whereas decreasing this ratio will produce longer products.

4. The synthesized cDNA should be stored at -20°C.

Item#:
ASCDNART3
While Supplies Last!


This brand is being discontinued and will only be available while supplies last. 

Need great dNTPs at a great price?

Try our PR1MA™ dNTPs!


 Bullseye Individual dNTP's

  • Ready-to-use molecular grade dNTP solution for use in DNA polymerization, DNA labeling and sequencing processes
  • High purity: >98% by HPLC
  • Supplied in solution at pH 7.5
  • dNTPs are stable at -20°C, avoid multiple freeze/thawing (For long-term usage, aliquoting is recommended)
  • Functionally tested with thermostable polymerases

Item#:
ASPCRDNTP4
While Supplies Last!

This brand is being discontinued and will only be available while supplies last.
 

Need a great DNA Safe Stain at a great price?
Try PR1MA! Click
 
here
 to order.
 
Bullseye DNA Safe Stain Plus

  • Higher sensitivity
  • Use in the same way as EtBr in agarose gel electrophoresis
  • Detection of DNA and RNA
  • Safest DNA stain by far
  • Low cost
  • 10,000X
  • Excitation wavelengths at 290nm and 490nm

DNA SafeStain Plus is a highly sensitive green fluorescent DNA/RNA staining reagent for detecting nucleic acids in agarose and polyacrylamide gels. This unique stain gives high sensitivity for detection of double-stranded or single-stranded DNA and RNA. Gels can be post-stained or the stain can be added to gels during gel casting or to the gel running buffer. DNA SafeStain Plus has two excitation wavelength peaks at about 290nm and 490nm, and an emission wavelength at 530nm, making it compatible with a standard UV light box, a blue-light transilluminator, or a gel reader equipped with visible light excitation; such as, a 488 nm laser-based gel scanner.


DNA SafeStain Plus is in a 10,000X concentrated format that can be easily diluted 10,000 times for use in precast gel staining, or 5,000 times for use in post gel staining.

Samples stained with DNA SafeStain Plus are compatible with downstream molecular biology applications; such as, gel extraction, and cloning.
 


EZ Pack Agarose Tablets

  • Eliminates weighing
  • Fast dissolving, just two minutes
  • Environmentally friendly, free from organic solvents
  • Consistent, reproducible gels
  • Enhanced resolution and clarity 

Researchers trust Benchmark’s Agarose LE to meet their electrophoretic needs for various applications. Now, the same agarose is available in a convenient, no-mess tablet.


Agarose LE is refined in an advanced process that excludes the use of organic solvents. The result is a cleaner end product with significantly reduced environmental impact. The agarose can be used for analyses of nucleic acids from 150 bp to 25,000 bp, protein electrophoresis, and various blotting protocols.


The low EEO of the agarose promotes increased electrophoretic mobility, yielding improved resolution and shorter run times. This also allows macromolecules and larger particles (subcellular fragments, viruses, etc.) to migrate more freely through the gel matrix. The consistently low EEO reduces band distortion (caused by counterflow) that can result from the presence of excessive sulfate-rich negative ions. The quick-dissolving EZ Pack™ tablet contains 0.5 g (500 mg) of Agarose LE, eliminating the hands-on time and inaccuracies normally associated with weighing. Use of the tablet is not only convenient and cleaner, but it also provides better consistency and reproducibility gel to gel.

 

Gel preparation is simple – add the desired number of tablets to the electrophoresis buffer, allow it to sit for two minutes, and then heat and pour as usual. The resulting gels are highly transparent, have exceptional thermal stability (ensuring safe and easy handling), and exhibit exceptionally low absorption of chemical staining agents.

EZ Pack™ Agarose Tablets are supplied in convenient blister packs for safe, clean dispensing.

 

Specifications
 

Gel Temperature36°C ± 1.5°C (1.5%)
Melt Temperature88°C ± 1.5°C (1.5%)
EEO (-mr)< 0.13
Moisture Content< 10%
Sulfate< 0.2%
RNase/DNaseNone Detected
Protease/EndonucleaseNone Detected
Storage ConditionsRoom Temperature
Gel Strength> 1200 g / cm2 (1%)
> 2500 g / cm2 (1.5%)
 
Buffer volume required to achieve desired gel strength
GEL %0.8%1.0%1.2%1.3%1.5%1.8%2.0%
1 Tab63 mL50 mL42 mL38 mL33 mL28 mL25 mL
2 Tabs125 mL100 mL83 mL77 mL67 mL56 mL50 mL
3 Tabs188 mL150 mL125 mL115 mL100 mL83 mL75 mL

Item#:
ASAGROTBLTS


Citric Acid, Monohydrate 

  • Appearance (Color): Colorless or White
  • Appearance (Form): Crystals
  • Purity: 99.0 - 102.0%
  • Identification (FTIR): Conforms to Structure
  • Water: 7.5 - 8.8% 
  • Lead: ≤ 3 ppm
  • Iron: ≤ 3 ppm
  • Oxalate: To Pass Test
  • Sulfate: ≤ 20 ppm
  • Chloride: ≤ 10 ppm
  • Readily Carbonizable Substances: Passes Test
  • Insoluble Matter: ≤ 0.005%
  • Residue After Ignition: ≤ 0.02%
  • DNase: None Detected
  • RNase: None Detected

*Custom sizes available upon request.

 

DOT Information: Non-regulated.
 

Item#:
ASCACIDMONO


Sodium Bicarbonate

  • Appearance: White Crystalline Powder
  • Purity: 99.0 - 100.5%
  • pH (5% Aqueous): 7.9 - 8.4
  • Water: ≤ 0.25%
  • Lead: ≤ 5 ppm
  • Arsenic: ≤ 2 ppm
  • Chloride: ≤ 150 ppm
  • Sulfate: ≤ 150 ppm
  • RNase: None Detected
  • DNase: None Detected

*Custom sizes available upon request.

 

DOT Information: Non-regulated.   
 

Item#:
ASBICARBSODIUM
Discontinued, Contact us for more options!


These items have been discontinued by the manufacturer.

See our MagBio HighPrep Plant DNA Plus Kits or contact us for more options.


PrecisionPak Plant Matter DNA Kit

 

All-inclusive kit, from lysis to extraction, including protocol, lysis beads, all buffers and reagents, to ensure high quality DNA.

 

The PrecisionPak Plant Matter DNA extraction kit contains a combination of lysis beads preloaded in sample tubes and lysis buffer for thorough homogenization and high yield. The buffers' formulations are environmentally friendly and do not require ethanol, phenol, chloroform, and isopropanol. The extraction kit is innovatively designed to be faster and more efficient than spin-column methods.

 

Tough Plant Matter DNA Kit available for: Barley, Beans, Blueberry, Cannabis, Chickpeas, Cloves, Conifer Needles, Corn, Dried Soy Beans, Fungi (M.phaseolina), Ginger Rhizome, Horseradish Root, Leaves, Leek, Malanga (Tuber), Microsporidia, Moss, Mung Beans, Mycelia, N. benthamiana, Pine Nut, Potato, Rice, Soy Bean Plant, Spelt, Sugar Cane Pulp, Sunflower Seeds, Sorghum, Tobacco, Tomato Root, Tomato Seeds, Wheat Berries.

 

Soft Plant Matter DNA Kit available for: Algae, A thaliana, and Phytoplankton.   
 

Item#:
ASPPPMDNAKIT


Guanidine Hydrochloride

  • Appearance: White Crystalline Powder
  • Purity: ≥ 99.0%
  • Solubility (6M Aqueous): Clear and Colorless
  • pH: 5.0 - 7.0
  • Identity (FTIR): Conforms to Structure
  • Water: ≤ 0.3%
  • Heavy Metals (as Fe): ≤ 5 ppm
  • A260 (6M Aqueous): ≤ 0.10
  • A280 (6M Aqueous) ≤ 0.05
  • RNase: None Detected
  • DNase: None Detected

*Custom sizes available upon request.

 

DOT Information: Non-regulated.   
 

Item#:
ASGUANIDINEHYDRO1

IBI Ethanol (Anhydrous Alcohol)

 

Introducing our premium-grade Ethanol, also known as Anhydrous Alcohol – the versatile solution for a myriad of applications. Sourced and refined with meticulous care, our Ethanol stands as a hallmark of purity and quality, ready to meet your diverse needs.

 

Our Ethanol is widely used for precipitating nucleic acids. The nucleic precipitate, which is formed in the presence of moderate concentrations of monovalent cations, is recovered by centrifugation and re-dissolved in an appropriate buffer at the desired concentration.

 

200 Proof Ethanol is denatured with methyl alcohol. It is also known as ethyl alcohol, alcohol anhydrous, denatured alcohol.

 

Specifications

 

CAS#: 64-17-5

200 Proof Ethanol denatured with 5% methanol

Used for precipitating nucleic acids

Specific Gravity: 0.7964 Max.
Formula Weight: 46.07
Molecular Formula: C2H5OH
Ethanol: 95%
Methanol: 5%
Moisture (KF): 1% Max.
Identification (IR): Pass


Molecular Biology Specifications

DNase assay: None Detected
RNase assay: None Detected

 

This product cannot be shipped to a personal residence

 

 

IBI Cell Culture Grade, Pyrogen/Endotoxin Free Water is prepared for nuclear transfer, transfection, transformation, cell and tissue culture,
LAL testing, and all other aqueous solution preparations that require stringent quality control.


IBI Cell Culture Grade Water is tested for use in critical assays and applications. The water is endotoxin-free (to the maximum detection
limit of <0.005EU/ml by turbidimetric assay). The purification process of our Cell Culture Grade Water includes distillation, continuous
deionization, reverse osmosis, 0.1µm filtration, followed by steam sterilization in an autoclave.


IB42010

Cell Culture Grade Water, Pyrogen and Endotoxin Free, 1L

IB42011

Cell Culture Grade Water, Pyrogen and Endotoxin Free, 6 x 1L

IB42012

Cell Culture Grade Water, Pyrogen and Endotoxin Free, 12 x 1L

IB42020

Cell Culture Grade Water, Pyrogen and Endotoxin Free, 2L

IB42021

Cell Culture Grade Water, Pyrogen and Endotoxin Free, 6 x 2L

IB42030

Cell Culture Grade Water, Pyrogen and Endotoxin Free, 10L

Item#:
ASMOLWATER

VitroINK® Bioinks

Ready-to-use bioinks for 3D bioprinting

VitroINK® are ready-to-use, xeno-free (animal origin-free) bioink system either unmodified or modified with either RGD, Collagen-memetic, IKVAV, or YIGSR peptides or with Matrix Metalloproteinases (MMP) for biodegradable bioink.

VitroINK® is a family of the ready-to-use, xeno-free tunable bioink system that requires no UV,  no temperature/pH curing, or chemical cross-linking. The system is ready-to-use at room temperature, neutral in pH, transparent, and has excellent visibility after printing and cell culture. Due to the unique shear-thinning and rapid recovery mechanical property, VitroINK® can maintain the printed structure without UV or other special curing methods. Adding cell culture medium after printing can further stabilize the printed structure and support cell growth. Cells can be pre-mix with VitroINK® using our VitroINK® Mixing Kit for mixing ratios at 3:1 or 10:1. Different versions of VitroINK® may incorporate multiple biological functional ligands to promote cell attachment, cell-matrix interactions, cell proliferation, motility/migration and differentiation for many different applications.


Specifications

  • Xeno-free tunable modified bioink.
  • Ready-to-use at room temperature
  • No UV, temperature/pH curing, or chemical cross-linking required
  • Neutral pH
  • Transparent. Excellent visibility after printing and cell culture
  • Pre-mix with cells using the included VitroINK® Mixing Kit
  • Ships room temperature. Store at 2-8°C
  • Size: 3 mL


TheWell products are never to be shipped to residential addresses. This decision has been made to safeguard the improper use and application of these products, particularly in the case of injectables and cell therapy treatments. TheWell has the right to refuse any orders that deem unfit use of their products or violate TheWell’s Terms of Use.   

 

TheWell products are sold for Laboratory Research Use Only, Not For Diagnostic or Therapeutic use, and are not to be administered to humans.

To ensure a seamless shopping experience, please provide a non-residential shipping address during checkout where your order can be safely received and stored.

  

Item#:
ASVITROINK

MagBio HighPrep Viral/Pathogen DNA/RNA Kit


Magnetic beads based kit for rapid isolation of viral, bacterial and fungal nucleic acids from whole blood, serum, plasma, saliva and other body fluids. 


Applications

Viral/Pathogen RNA and DNA isolation for:

  •     RT-qPCR; RT-PCR, PCR
  •     One-Step RT-qPCR
  •     Virus detection, genotyping
  •     Viral load monitoring,

Benefits

  •     OPTIMIZED FOR ISOLATION from FUNGAL, BACTERIAL and VIRAL samples.
  •     Rapid and reliable purification of nucleic acids
  •     Adaptable to various automated liquid handling workstations
  •     No toxic organic solvents
 

The HighPrep™ Viral/Pathogen DNA/RNA kit is designed for rapid and reliable isolation of viral, bacterial and fungal nucleic acids from whole blood, serum, plasma, saliva and other body fluids as well as nasopharyngeal swabs soaked in virus transport media or other buffers. This kit is highly efficient in vIral nucleic acid isolation and the extracted RNA (and DNA) is suitable for direct use in most downstream applications such as one-step RT-qPCR, RT-PCR, PCR, nucleic acid amplification, cloning, sequencing, and enzymatic reactions. The kit can be used in low throughput manual workflows and is also adaptable to majority of the liquid handling workstations in the market. 

Item#:
ASHIHPRPVIRPATDK
|◀ 133 - 144 of 434 ▶|
View: