QuantiChrom™ Protein Assay Kit

SKU:BHT15600233
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BioAssay Systems
BioAssay Systems
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Overview
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QuantiChrom Protein Assay Kit is designed for quantitative determination of total protein. It uses OD595 nm (Bradford) readout; suited to biological, food, agriculture; typical assay time 2 min; detection limit 60 µg/mL.
Detection method Colorimetric (OD 595 nm)
Sample type Biological, food, agriculture etc
Species All species
Procedure 2 min
Detection limit 60 µg/mL
Options selector
Catalog no. Size
QCPR-500 500 Tests
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 500 Tests
  • Lead time: varies by selected option; please contact us for current fulfillment timing.
  • Storage: -20°C — Store at -20°C (freezer). Avoid repeated freeze-thaw cycles.
  • Shipping: cold-chain shipment (typically with ice packs).
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Species All
Applications
  • Functional Assay (In Vitro)
Sample type(s) Biological, food, agriculture etc
Detection limit 60 µg/mL
Detection method
  • Colorimetric (OD 595 nm)
Plate format 96-well plate
Assay time
  • 2 min
Storage -20°C — Store at -20°C (freezer). Avoid repeated freeze-thaw cycles.
Shelf life 12 Months
Shipping Ambient (RT) — Ships at room temperature. No cold pack required.
Catalog no. (Mfr.) QCPR-500
Main SKU BHT15600233

Overview

For quantitative determination of total protein. The assay uses OD595nm (Bradford) for signal readout. Compatible sample input includes Biological, food, agriculture etc. Typical stated assay timing is 2 min.

Key elements and design rationale

  • Readout format: OD595nm (Bradford) supports plate-based signal acquisition and consistent comparison across matched samples.
  • Sample compatibility: The stated sample scope includes Biological, food, agriculture etc, which is useful when aligning matrix type with calibration and control design.
  • Analytical range context: The supplied specifications include a stated detection limit of 60 µg/mL for interpreting low-signal samples.
  • Feature emphasis: Sensitive and accurate. Use 10 mL samples. Detection range 0.06 – 1.0 mg /mL protein in 96-well plate assay.

Additional feature notes highlight Simple and high-throughput. The “mix-and-read” procedure involves addition of a single working reagent and reading the optical density. Can be readily automated as a high-throughput assay in 96-well plates for thousands of samples per day; Low interference. Glucose, Tris, vitamins, and amino acids, DNA, RNA, salts, EDTA (< 12 mM), phenol (< 50 mM), urea (< 0.6 M), Triton (<0.1%) and SDS (< 0.1% SDS) do not interfere in the assay. Available format information for this listing includes 500 Tests.

Biological background

This product is centered on measurement of protein within the matrices described for the assay. In practice, datasets from this type of format are typically interpreted by comparing relative signal, activity, or abundance across matched control and experimental groups rather than relying on a single value in isolation. Careful alignment of sample matrix, incubation window, and calibration strategy is important when comparing results across plates, operators, or study days.

More details

The protein is known as the “building blocks of life” and is one of the most important macromolecules in life science. Proteins are polypeptides made up of amino acids and play various key roles in all aspects of biology. Protein quantitation is a very common practice for life scientists. Simple, direct and automation-ready procedures for measuring protein concentration are very desirable. BioAssay Systems QuantiChrom™ protein assay kit is based on an improved Coomassie Blue G method. The dye forms a blue complex specifically with protein, and the intensity of color, measured at 595nm, is directly proportional to the protein concentration in the sample. The optimized formulation substantially reduces interference by substances in the raw samples and exhibits increased sensitivity towards peptides.

Detection method

Colorimetric (OD 595 nm).

Detection limit and analytical sensitivity

Reported detection limit: 60 µg/mL.

Procedures and timing

Stated procedure or timing information: 2 min.

Research relevance and current trends

  • Plate-based quantification and side-by-side group comparison remain central use cases for this assay format.
  • The product notes emphasize multi-sample throughput, making it relevant for screening-oriented and larger batch comparison studies.
  • Short assay timing and plate compatibility support time-course or repeated-measure collection plans when handling is kept consistent.

Common research applications

  • Quantify protein in biological, food, agriculture by OD595 nm (Bradford) readout.
  • Compare treatment or phenotype groups using matched biological, food, agriculture handling.
  • Monitor time-course or pre/post changes in biological, food, agriculture across study conditions.

Interpretation is usually strongest when signal changes are assessed alongside matrix-matched controls, replicate agreement, and the assay's stated analytical window.

Notes for experimental interpretation

  • Matrix composition, background signal, and sample handling can influence apparent response; compare like-with-like whenever possible.
  • Use appropriate blanks, controls, and replicate wells to distinguish biological differences from plate, reagent, or handling variability.
Your protein assay kit detection range is 60-1000 µg/ml, is it possible to improve the kit sensitivity?

Simply adding 50 μL sample to 200 μL reagent increases the sensitivity to 3-200 mg/mL protein.

For laboratories requiring additional technical capacity, we provide scientific support services including assay execution, method guidance, product sourcing, and customization to align the assay with specific experimental objectives. If you need assistance selecting the appropriate kit configuration, adapting the workflow to your application, or identifying related research services, please click Talk to a Scientist, email support@biohippo.com, or review our Research Services; a member of our scientific team will follow up with recommendations tailored to your study.

Metabolic activities and chondrogenic differentiation of human mesenchymal stem cells following recombinant adeno-associated virus-mediated gene transfer and overexpression of fibroblast growth factor 2

Cucchiarini M et al (2011). Metabolic activities and chondrogenic differentiation of human mesenchymal stem cells following recombinant adeno-associated virus-mediated gene transfer and overexpression of fibroblast growth factor 2. Tissue Eng Part A. 17(15-16):1921-33. Assay: Protein in bacteria p450 enzymes.

Subcellular components of probiotics Kocuria SM1 and Rhodococcus SM2 induce protective immunity in rainbow trout (Oncorhynchus mykiss, Walbaum) against Vibrio anguillarum

Sharifuzzaman SM et al (2011). Subcellular components of probiotics Kocuria SM1 and Rhodococcus SM2 induce protective immunity in rainbow trout (Oncorhynchus mykiss, Walbaum) against Vibrio anguillarum. Fish Shellfish Immunol. 30(1):347-53. Assay: Protein in human urine.

Subcellular components of probiotics Kocuria SM1 and Rhodococcus SM2 induce protective immunity in rainbow trout (Oncorhynchus mykiss, Walbaum) against Vibrio anguillarum

Sharifuzzaman SM, et al (2011). Subcellular components of probiotics Kocuria SM1 and Rhodococcus SM2 induce protective immunity in rainbow trout (Oncorhynchus mykiss, Walbaum) against Vibrio anguillarum. Fish Shellfish Immunol. 30(1):347-53. Assay: Protein in bacteria cells.

Some Biochemical Characteristics and Preservation of Epididymal Camel Spermatozoa (Camelus dromedarius)

Waheed MM, et al (2011). Some Biochemical Characteristics and Preservation of Epididymal Camel Spermatozoa (Camelus dromedarius). Theriogenology 76(6):1126-33. Assay: Protein in animal testicles.

Limb regeneration is impaired in an adult zebrafish model of diabetes mellitus

Olsen AS et al (2010). Limb regeneration is impaired in an adult zebrafish model of diabetes mellitus. Wound Repair Regen. 18(5):532-42. Assay: Protein in rat tissue.

Kocuria SM1 controls vibriosis in rainbow trout (Oncorhynchus mykiss, Walbaum)

Sharifuzzaman SM, Austin B (2010). Kocuria SM1 controls vibriosis in rainbow trout (Oncorhynchus mykiss, Walbaum). J Appl Microbiol. 108(6):2162-70. Assay: Protein in fish serum.

Kocuria SM1 controls vibriosis in rainbow trout (Oncorhynchus mykiss, Walbaum)

Sharifuzzaman SM, Austin B (2010). Kocuria SM1 controls vibriosis in rainbow trout (Oncorhynchus mykiss, Walbaum). J Appl Microbiol. 108(6):2162-70. Assay: Protein in rat tissue.

Evaluation of the efficacy of yeast extract in reducing intestinal Clostridium perfringens levels in broiler chickens

Thanissery R et al (2010). Evaluation of the efficacy of yeast extract in reducing intestinal Clostridium perfringens levels in broiler chickens. Poult Sci. 89(11):2380-8. Assay: Protein in rat brown fat tissue.

Probing the role of the proximal heme ligand in cytochrome P450cam by recombinant incorporation of selenocysteine

Aldag C et al (2009). Probing the role of the proximal heme ligand in cytochrome P450cam by recombinant incorporation of selenocysteine. PNAS 106(14):5481-6. Assay: Protein in Bacteria cells.

Influence of probiotic feeding duration on disease resistance and immune parameters in rainbow trout

Sharifuzzaman SM, Austin B (2009). Influence of probiotic feeding duration on disease resistance and immune parameters in rainbow trout. Fish Shellfish Immunol. 27(3):440-5. Assay: Protein in fish.

The role of thermogenesis in antipsychotic drug-induced weight gain

Stefanidis A, et al (2009). The role of thermogenesis in antipsychotic drug-induced weight gain. Obesity (Silver Spring) 17(1):16-24. Assay: Protein in rat brown fat tissue.

The effects of rimonabant on brown adipose tissue in rat: implications for energy expenditure

Verty AN, et al (2009). The effects of rimonabant on brown adipose tissue in rat: implications for energy expenditure. Obesity (Silver Spring) 17(2):254-61. Assay: Protein in rat tissue.

2007 AAPS Annual Meeting & Exposition

Lai, M. et al (2007). 2007 AAPS Annual Meeting & Exposition. Development of an In-Vitro Screening Method to Determine Enzymatic Release rates from a Homologous Series of Novel SN-38 Conjugates. Sonus Pharmaceuticals. Assay: Protein in rat tissue.

Effects of Long-term Strenuous Exercise onOxidative DNA Damage and Proteinuria in humans

Yasuda, N (2007). Effects of Long-term Strenuous Exercise onOxidative DNA Damage and Proteinuria in humans. GraduateStudent Theses, Dissertations, & Professional Papers. 362. Assay: DNA in rat primary glial culture.

Effects Of Long-Term Strenuous Exercise On Oxidative Dna Damage And Proteinuria In humans

Yasuda, N. (2007). Effects Of Long-Term Strenuous Exercise On Oxidative Dna Damage And Proteinuria In humans. Ph.D. Thesis. Assay: Protein in human urine.

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