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chromatography+columns+HyClone+products+(Cytiva)


72,343  results were found

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Supplier:  Bioss
Description:   Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf56 gene product has been provisionally designated C18orf56 pending further characterization.
Supplier:  KEYSTONE ADJUSTABLE CAP CO., INC.
Description:   Self-Sealing 1073B Tyvek® are ideal for steam sterilization of pharmaceutical components such as vial and syringe stoppers and caps as well as heavy equipment parts with sharp edges. No need to use or validate a heat sealing machine.
Supplier:  AGILENT TECHNOLOGIES, INC (CSD) CA
Description:   Stainless steel capillaries and tubing for selected Thermo Fisher Scientific HPLC systems.
Supplier:  Kent
Description:   Free-Band® Disposable Tourniquets are manufactured from soft and durable proprietary blend of thermoplastic materials specifically chosen to provide physical properties that closely resemble latex and performance without the worry of latex allergens.
Catalog Number: (10101-826)

Supplier:  Prosci
Description:   ZNF132 may be involved in transcriptional regulation.

Supplier:  Prosci
Description:   The exact function of LOC653135 remains unknown.

Supplier:  Prosci
Description:   The exact function of LOC727817 remains unknown.
Supplier:  LIFE TECHNOLOGIES CORP CA
Description:   Thermo Scientific Pierce CDI-Activated Agarose is carbonyldiimidazole affinity chromatography resin, activated for covalent immobilization of N-nucleophiles and primary amine ligands in aqueous or organic solvent conditions.
MSDS SDS
Supplier:  Electron Microscopy Sciences
Description:   This mounting medium is made with limonene, a natural product from orange peels. It preserves  tissues and cell smears that can be dehydrated with organic solvents in immunohistochemistry, e.g. DAB and DAB with nickel or cobalt.
Minority or Woman-Owned Business Enterprise
Supplier:  AGILENT TECHNOLOGIES, INC (CSD) CA
Description:   Sample tubes and vials for SPS 4, SPS 3, and ASX 500 autosamplers for AAS, ICP-OES, MP-AES and ICP-MS.
Catalog Number: (10104-376)

Supplier:  Prosci
Description:   The function of the C6orf199 protein remains unknown.
Catalog Number: (10104-310)

Supplier:  Prosci
Description:   The function of CCDC69 remains unknown.
Supplier:  IBI Scientific
Description:   The Large DNA Fragment Extraction Kits are designed to recover large DNA fragments (>8Kb) from an agarose gel
Catalog Number: (MSPP-781461006)

Supplier:  Stemcell Technologies
Description:   Interleukin 3 (IL-3) is a species-specific pleiotropic cytokine that promotes the survival and proliferation of pluripotent hematopoietic stem cells and lineage-committed progenitor cells and their differentiation into mature cells of most lineages, including basophils, neutrophils, eosinophils, macrophages, dendritic cells, erythrocytes, and megakaryocytes (Yang <i>et al.</i>; Dorssers <i>et al.</i>; Broughton <i>et al.</i>). IL-3 is produced by activated T cells and has a physiological role in inflammation and allergies by promoting the secretion of inflammatory mediators such as histamine, IL-4, and IL-6 by basophils and eosinophils (Broughton <i>et al.</i>). The IL-3 receptor consists of a unique alpha subunit (CD123) and a beta common subunit (βc or CD131) that is shared with the receptors for IL-5 and GM-CSF, and is the principal signal transduction subunit for these cytokines. IL-3 binding to the heterodimeric receptor activates JAK/STAT, MAPK, and PI3K signaling pathways (Woodcock <i>et al.</i>). This product is animal component-free.
New Product

Supplier:  Bioss
Description:   Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf54 gene product has been provisionally designated C18orf54 pending further characterization.
Supplier:  Bioss
Description:   C9orf5 (chromosome 9 open reading frame 5), also known as CG2, is a 911 amino acid multi-pass membrane protein that is widely expressed and exists as four alternatively spliced isoforms. The gene encoding C9orf5 maps to human chromosome 9, which consists of about 145 million bases, represents 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.
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