The main purpose of buffered salt solutions is the maintenance of pH and osmolarity in cell culture applications as well as providing essential inorganic ions. These solutions are usually used for washing tissues and cells. Often they are combined with other agents in cell and tissue treatment. Equivalent/Alternative to: Biochrom Cat.-no. L 1825

Intrinsically developed for the cultivation of murine embryonic cells, DMEM is tailor-made for the cultivation of a broad range of cells, especially if the medium is supplemented with FBS. DMEM is an Eagle medium modification with a fourfold content of amino acids and vitamins. DMEM with 1.0 g/L Glucose is the standard medium, whereas DMEM with 4.5 g/L Glucose is for cells which have a high energy demand.

Application For dissociation of tissue and cell monolayer cultures. Shelf life Solution 24 months, powder 36 months. The shelf life commences with date of production. Storage Solution at -20° C, powder at 2 - 8° C. Other sizes and custom formulation Please ask for other sizes or special formulations of trypsin; in most cases we can provide a solution. Our trypsin is tested negative for mycoplasma and PPV. Equivalent/Alternative to: Biochrom Cat.-no. L 2143

The medium was developed for culture of normal and neoplastic leukocytes, but also marrow cells and hybridoma cells. Meanwhile there are better, serum-free media for hybridoma cells such our Panserin H4000. Just by supplementing RPMI 1640 with varying amounts of FBS, a very good medium for many different cell lines can be obtained.

The medium was developed for culture of normal and neoplastic leukocytes, but also marrow cells and hybridoma cells. Meanwhile there are better, serum-free media for hybridoma cells such our Panserin H4000. Just by supplementing RPMI 1640 with varying amounts of FBS, a very good medium for many different cell lines can be obtained. Equivalent/Alternative to: Biochrom Cat.-no. FG 1215, FG 1415

Intrinsically developed for the cultivation of murine embryonic cells, DMEM is tailor-made for the cultivation of a broad range of cells, especially if the medium is supplemented with FBS. DMEM is an Eagle medium modification with a fourfold content of amino acids and vitamins. DMEM with 1.0 g/L Glucose is the standard medium, whereas DMEM with 4.5 g/L Glucose is for cells which have a high energy demand. Equivalent/Alternative to: Biochrom Cat.-no. F 0445

Intrinsically developed for the cultivation of murine embryonic cells, DMEM is tailor-made for the cultivation of a broad range of cells, especially if the medium is supplemented with FBS. DMEM is an Eagle medium modification with a fourfold content of amino acids and vitamins. DMEM with 1.0 g/L Glucose is the standard medium, whereas DMEM with 4.5 g/L Glucose is for cells which have a high energy demand.

Even though cells should be cultured without the addition of antibiotics or antifungal drugs, cell culture media are not only a perfect breeding ground for your cell culture but also for many contaminants, such as bacteria and fungi. In certain cases the addition of antibiotics is necessary (for unique cell lines or to remove already existing contamination). Equivalent/Alternative to: Biochrom Cat.-no. A 2213

In many cases the isolation of cells is the first step for gene expression studies or in diagnostic procedures. Besides biological separation techniques physical separation methods are most commonly used. These methods use physical differences such as size and weight of the particles to be separated. For this purpose so-called separating solutions (= centrifugation media) are used. These media must meet the following criteria: They must be able to form a density gradient over the desired range The desired pH value and osmolality must be easy to adjust The solutions must not be too viscous at high density They must not cause functional or morphological changes to biological materials They must not penetrate biological membranes Our Pancoll separating solutions contain a polysaccharide with a molecular weight of 400,000 daltons; this hydrophilic polymer allows for production of aqueous solutions for cell separation with a density of up to 1.2 g/ml. PAN-Biotech offers a variety of ready-to-use products with a density of 1.063 g/ml up to 1.091 g/ml for a very wide range of cell separation applications. Storage 2° C to ambient temperature "Protect from light!“ When properly stored, separating solutions are stable for at least 36 months. The storage period starts with the manufacturing date. Equivalent/Alternative to: Biochrom Cat.-no. L 6115

Intrinsically developed for the cultivation of murine embryonic cells, DMEM is tailor-made for the cultivation of a broad range of cells, especially if the medium is supplemented with FBS. DMEM is an Eagle medium modification with a fourfold content of amino acids and vitamins. DMEM with 1.0 g/L Glucose is the standard medium, whereas DMEM with 4.5 g/L Glucose is for cells which have a high energy demand. Equivalent/Alternative to: Biochrom Cat.-no. FG 0435

Cryopan III is a serum-free freezing medium without DMSO, suitable for the cryopreservation of various cell types. Key Features: Versatility: Cryopan III is a specially developed cryopreservation medium designed for freezing various human and animal cells. Its optimized formulation is suitable for preserving both adherent and suspension cells. It is ideal for the long-term storage of established cell lines, primary cells and tissue samples such as umbilical cord tissue. Composition: Cryopan III consists of a chemically defined and optimized mixture of salts, sugar and additional antifreeze-substances. It contains no animal or human components and is free of DMSO. Special Advantages: The formulation without DMSO is particularly well-suited for primary cells and other applications in which the cytotoxic side-effects associated with DMSO are not desired. The serum-free freezing medium is particularly well-suited for preserving serum-free cultured cells. The optimized composition guarantees high cell viability post-thawing.

RNase/DNase Neutralizer is a decontamination solution designed to completely eliminate RNase and DNase contamination from various labware and surfaces. It effectively removes even high levels of contaminants from glassware, single-use devices like reaction vessels, culture dishes, pipette tips, and microtiter plates. Key Features Versatility: RNase/DNase Neutralizer is also thoroughly tested for use on work surfaces, including lab benches and laminar flow hoods, providing reliable and comprehensive protection for laboratory environment. Composition: RNase/DNase Neutralizer is formulated with an optimized mixture of substances, each specifically chosen for its effectiveness against nucleases. This carefully selected combination of components ensures maximum activity and efficiency in inhibiting nucleases. Special Advantages: The use of DNA- and RNA-based pharmaceuticals is becoming an increasingly important research area for treating various diseases and developing vaccines. These innovative therapies and vaccines rely heavily on the purity and integrity of their nucleic acid components, making it essential to eliminate contamination from degrading enzymes like DNases and RNases to ensure their effectiveness and safety. RNase/DNase Neutralizer provides immediate and effective decontamination, even against high concentrations of RNase and DNase, ensuring optimal protection. Applications RNase/DNase Neutralizer is suitable for a broad range of applications: Molecular diagnostics PCR mixtures RNA and DNA sequencing Gene therapy CRISPR/CAS9 buffers In vitro transcription cDNA synthesis

RNase/DNase Neutralizer is a decontamination solution designed to completely eliminate RNase and DNase contamination from various labware and surfaces. It effectively removes even high levels of contaminants from glassware, single-use devices like reaction vessels, culture dishes, pipette tips, and microtiter plates. Key Features Versatility: RNase/DNase Neutralizer is also thoroughly tested for use on work surfaces, including lab benches and laminar flow hoods, providing reliable and comprehensive protection for laboratory environment. Composition: RNase/DNase Neutralizer is formulated with an optimized mixture of substances, each specifically chosen for its effectiveness against nucleases. This carefully selected combination of components ensures maximum activity and efficiency in inhibiting nucleases. Special Advantages: The use of DNA- and RNA-based pharmaceuticals is becoming an increasingly important research area for treating various diseases and developing vaccines. These innovative therapies and vaccines rely heavily on the purity and integrity of their nucleic acid components, making it essential to eliminate contamination from degrading enzymes like DNases and RNases to ensure their effectiveness and safety. RNase/DNase Neutralizer provides immediate and effective decontamination, even against high concentrations of RNase and DNase, ensuring optimal protection. Applications RNase/DNase Neutralizer is suitable for a broad range of applications: Molecular diagnostics PCR mixtures RNA and DNA sequencing Gene therapy CRISPR/CAS9 buffers In vitro transcription cDNA synthesis

WFI quality water is manufactured in our new GMP compliant facility. Every batch of PAN-Biotech WFI quality water is released based on EP (European Pharmacopoeia) and USP (United States Pharmacopoeia) specifications. Our WFI quality water is suitable for a broad variety of upstream and downstream applications.

WFI quality water is manufactured in our new GMP compliant facility. Every batch of PAN-Biotech WFI quality water is released based on EP (European Pharmacopoeia) and USP (United States Pharmacopoeia) specifications. Our WFI quality water is suitable for a broad variety of upstream and downstream applications.

Spodopan is a serum-free and protein-free medium for optimized growth of insect cells such as Sf9 and Sf21 (Spodoptera frugiperda) in suspension culture. Composition Spodopan contains amino acids, vitamins, salts, trace elements, lipids and growth promoting factors in a formulation optimized for insect cells. It contains no protein or any other components of human or animal origin, only traces of animal-derived components (< 0.2 % w/v) and hydrolysates (< 0.7 % w/v). Suitability Spodopan is suitable for the cultivation of insect cells and the production of recombinant proteins and viruses (Baculovirus expression vector system, BEVS).