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chromatography+columns+HyClone+products+(Cytiva)


72,344  results were found

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Supplier:  PeproTech, Inc.
Description:   Produced from sera of rabbits immunized with highly pure Recombinant Rat TNF-α. Anti­Rat TNF-α­specific antibody was purified by affinity chromatography employing an immobilized Rat TNF-α matrix.
Supplier:  PeproTech, Inc.
Description:   Produced from sera of goats immunized with highly pure Recombinant Human IL-6. Anti­Human IL-6­specific antibody was purified by affinity chromatography employing an immobilized Human IL-6 matrix.
Supplier:  PeproTech, Inc.
Description:   Produced from sera of goats immunized with highly pure Recombinant Human IL-2. Anti­Human IL-2­specific antibody was purified by affinity chromatography employing an immobilized Human IL-2 matrix.
Supplier:  MilliporeSigma
Description:   These reagents are produced using specially selected distillation methods that ensure consistently high dryness and batch-to-batch consistency. To protect the quality of these products even better from potential contaminants, a septum seal cap provides multiple layers of protection to keep solvents in flawless condition before, during, and after removal.
MSDS SDS
Supplier:  PeproTech, Inc.
Description:   Produced from sera of rabbits immunized with highly pure Recombinant Murine C10 (CCL6). Anti­Murine C10 (CCL6)­specific antibody was purified by affinity chromatography employing an immobilized Murine C10 matrix.
Supplier:  New England Biolabs (NEB)
Description:   The Monarch® RNA Cleanup Columns (50 µg) are a component of the Monarch® RNA Cleanup Kit (50 µg) and can be used to purify up to 50 µg of RNA from enzymatic reactions. 
Supplier:  Diagnostic Biosystems
Description:   Uroplakins (UPs) are a family of transmembrane proteins (UPs Ia, Ib, II and III) that are specific differentiation products of urothelial cells. In non-neoplastic mammalian urothelium, UPs are expressed in the luminal surface plasmalemma of superficial (umbrella) cells, Uroplakin II/III cocktail is specific for tumors of urothelial origin and, when used in combination with other markers, can aid in the diagnosis of primary and metastatic tumors.

Supplier:  Ceodeux Inc.
Description:   Used for instrumentation, hydraulic pipes, pneumatic pipes, chromatography, control panels, moderate, vacuum systems, chemical research, gas analysis, etc.
Supplier:  PeproTech, Inc.
Description:   Produced from sera of rabbits immunized with highly pure Recombinant Human SCF. Anti­Human SCF­specific antibody was purified by affinity chromatography employing an immobilized Human SCF matrix.
Supplier:  PeproTech, Inc.
Description:   Produced from sera of rabbits immunized with highly pure Recombinant Rat IL-2. Anti­Rat IL-2­specific antibody was purified by affinity chromatography employing an immobilized Rat IL-2 matrix.
Supplier:  PeproTech, Inc.
Description:   Produced from sera of rabbits immunized with highly pure Recombinant Murine IL-6. Anti­Murine IL-6­specific antibody was purified by affinity chromatography employing an immobilized Murine IL-6 matrix.

Supplier:  PeproTech, Inc.
Description:   Produced from sera of rabbits immunized with highly pure Recombinant Human Oncostatin M. Anti­Human Oncostatin M­specific antibody was purified by affinity chromatography employing an immobilized Human Oncostatin M matrix.

Supplier:  Bioss
Description:   The protein encoded by this gene belongs to the SMAD, a family of proteins similar to the gene products of the Drosophila gene 'mothers against decapentaplegic' (Mad) and the C. elegans gene Sma. SMAD proteins are signal transducers and transcriptional modulators that mediate multiple signaling pathways. This protein mediates the signals of the bone morphogenetic proteins (BMPs), which are involved in a range of biological activities including cell growth, apoptosis, morphogenesis, development and immune responses. In response to BMP ligands, this protein can be phosphorylated and activated by the BMP receptor kinase. The phosphorylated form of this protein forms a complex with SMAD4, which is important for its function in the transcription regulation. This protein is a target for SMAD-specific E3 ubiquitin ligases, such as SMURF1 and SMURF2, and undergoes ubiquitination and proteasome-mediated degradation. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq].

Supplier:  Bioss
Description:   This gene encodes a 105 kD protein which can undergo cotranslational processing by the 26S proteasome to produce a 50 kD protein. The 105 kD protein is a Rel protein-specific transcription inhibitor and the 50 kD protein is a DNA binding subunit of the NF-kappa-B (NFKB) protein complex. NFKB is a transcription regulator that is activated by various intra- and extra-cellular stimuli such as cytokines, oxidant-free radicals, ultraviolet irradiation, and bacterial or viral products. Activated NFKB translocates into the nucleus and stimulates the expression of genes involved in a wide variety of biological functions. Inappropriate activation of NFKB has been associated with a number of inflammatory diseases while persistent inhibition of NFKB leads to inappropriate immune cell development or delayed cell growth. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009].
Supplier:  Bioss
Description:   C9orf30 is a 275 amino acid protein that is expressed in brain and belongs to the UPF0439 family. The gene encoding C9orf30 maps to human chromosome 9q31.1. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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.
Supplier:  Bioss
Description:   Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf31 gene product has been provisionally designated C8orf31 pending further characterization.
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