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chromatography+columns+HyClone+products+(Cytiva)
Supplier:
Bel-Art Products
Description:
Filter large volumes quickly with a polyethylene plastic Table-Top Buchner Funnel using your choice of Fritware® or Perforated filter plate.
Catalog Number:
(76461-872)
Supplier:
Berkshire
Description:
Lightweight, high absorbency material design reduces actual cost in use compared to heavier weight products.
Supplier:
Restek
Description:
Topaz GC inlet liners feature revolutionary technology and inertness to deliver you the next level of True Blue Performance.
Catalog Number:
(CA76634-476)
Supplier:
Diagnostic Biosystems
Description:
The Bcl-2 product is considered to act as an inhibitor of apoptosis. Bcl-2 expression is inhibited in germinal centers where apoptosis forms part of the B cell production pathway. Reactive follicles show no staining for Bcl-2, whereas the cells in neoplastic follicles exhibit membrane staining. Bcl-2 α oncoprotein has been shown to inhibit apoptosis.
Supplier:
Mortech Manufacturing
Description:
Mopec’s range of Harmony tissue marking dyes are used to permanently mark surgical tissue margins in Histological specimens. Marking dyes are available in nine colors, with a standardized viscosity over the range. This ensures that there is less variation in viscosity from one color to another as compared to competitor products and allows the easy marking of both small and large specimens with any chosen color.
Catalog Number:
(30617-648)
Supplier:
Bel-Art Products
Description:
Sturdy corrugated cardboard receptacle is supplied with a 2 mil thick, clear polyethylene bag to contain broken glass fragments and spilled liquids.
Catalog Number:
(70680-452)
Supplier:
Bel-Art Products
Description:
The body is Teflon® PTFE with a Viton® O-Ring and is designed for use with 10 mm stirring rods.
Supplier:
Trajan Scientific and Medical
Description:
SGE autosampler syringes feature Diamond Syringe Technology
Catalog Number:
(76474-658)
Supplier:
Transforming Technologies
Description:
Anti-Static and ESD curtains are a great way to separate critical workspaces while also attending to the static-sensitive nature of certain products.
Catalog Number:
(76120-402)
Supplier:
Bioss
Description:
Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf112 gene product has been provisionally designated C20orf112 pending further characterization.
Catalog Number:
(76119-300)
Supplier:
Bioss
Description:
Ribonucleotide reductase is essential for the production and maintenance of the level of deoxyribonucleoside triphosphates (dNTPs) required for DNA synthesis. It is an enzymatic complex consisting of two nonidentical subunits, R1 and R2, which are inactive separately. R2, the smaller subunit, is localized to the cytoplasm. R2 is the limiting factor of the catalytic activity of the ribonucleotide reductase enzymatic complex. R2 expression is strictly correlated to the S-phase of the cell cycle, whereas R1 remains constant throughout all phases of the cell cycle. While R2 seems to be involved solely in the maintenance of dNTPs for DNA replication, a similar protein, p53R2, has been shown to be responsible for the production of dNTPs in response to DNA damage.
Catalog Number:
(76120-444)
Supplier:
Bioss
Description:
The gene encoding C20orf141 maps to human chromosome 20, which houses over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought important for seminal production and may be potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. The C20orf141 gene product has been provisionally designated C20orf141 pending further characterization.
Catalog Number:
(76120-416)
Supplier:
Bioss
Description:
Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf19 gene product has been provisionally designated C20orf19 pending further characterization.
Catalog Number:
(17308-050)
Supplier:
Bel-Art Products
Description:
These 7.6 liter (8qt.) plastic pails are available in polyethylene or autoclavable polypropylene.
Supplier:
Shenandoah Biotechnology
Description:
Macrophage inflammatory protein-1 beta (MIP-1 β), also known as CCL4, is produced by macrophages and functions as a mitogen-inducible cytokine. MIP-1 β signals through the chemokine receptor CCR5 to chemoattract immune cells. MIP-1 β induces inflammatory responses, including neutrophil superoxide production. The MIP-1 β and MIP-1 α heterodimer exhibits antiviral activity against the human immunodeficiency virus 1 (HIV-1).
Catalog Number:
(76099-566)
Supplier:
Bioss
Description:
Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf66 gene product has been provisionally designated C9orf66 pending further characterization.
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