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chromatography+columns+HyClone+products+(Cytiva)
Catalog Number:
(10855-874)
Supplier:
Restek
Description:
Replacement Transfer Line, for EZ No-Vent* GC Column-Mass Spectrometer Connectors, 3FT
Catalog Number:
(76120-578)
Supplier:
Bioss
Description:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf61 gene product has been provisionally designated C12orf61 pending further characterization.
Catalog Number:
(10401-932)
Supplier:
Bioss
Description:
Receptor that mediates the recognition, internalization and degradation of oxidatively modified low density lipoprotein (oxLDL) by vascular endothelial cells. OxLDL is a marker of atherosclerosis that induces vascular endothelial cell activation and dysfunction, resulting in pro-inflammatory responses, pro-oxidative conditions and apoptosis. Its association with oxLDL induces the activation of NF-kappa-B through an increased production of intracellular reactive oxygen and a variety of pro-atherogenic cellular responses including a reduction of nitric oxide (NO) release, monocyte adhesion and apoptosis. In addition to binding oxLDL, it acts as a receptor for the HSP70 protein involved in antigen cross-presentation to naive T-cells in dendritic cells, thereby participating in cell-mediated antigen cross-presentation. Also involved in inflammatory process, by acting as a leukocyte-adhesion molecule at the vascular interface in endotoxin-induced inflammation. Also acts as a receptor for advanced glycation end (AGE) products, activated platelets, monocytes, apoptotic cells and both Gram-negative and Gram-positive bacteria.
Catalog Number:
(76007-120)
Supplier:
Remco Products
Description:
Stainless steel blade removes stubborn dirt and other substances. Block material is polypropylene; blade material is stainless steel.
Supplier:
BioFit
Description:
BioFit multipurpose carts are specially designed to transport and store media, equipment and supplies in a variety of work and training spaces.
Supplier:
Bel-Art Products
Description:
Clear acrylic plastic animal restrainers have removable head and tail gates.
Catalog Number:
(89317-736)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to Cybr
Supplier:
Bel-Art Products
Description:
Griffin low-form polypropylene plastic beakers are translucent, chemical resistant, and will stack without sticking together.
Supplier:
AGILENT TECHNOLOGIES, INC (CSD)
Description:
Tubing and Fittings are designed for 8453 and 8454 UV-Vis Instruments and Accessories.
Catalog Number:
(CA89407-216)
Supplier:
HARDY DIAGNOSTICS CA
Description:
Pseudomonas Agar F, 18ml fill, 15x100mm plate, For the detection and differentiation of Pseudomonas aeruginosa by enhancement of fluorescein production. pack of 10
Catalog Number:
(470016-988)
Supplier:
Bel-Art
Description:
The Write-On™ tape dispensers make labeling easy and fast.
Catalog Number:
(75878-116)
Supplier:
BIOASSAY SYSTEMS
Description:
For quantitative determination of L-malate (L-malic acid) and drug effects on malate metabolism.
Supplier:
Teknova
Description:
Plate count agar are a standard method medium used for the enumeration of bacteria in water, waste water, dairy products and foods.
Supplier:
PIP
Description:
These gloves used for general handling, assembly, fabrication, parts handling and maintenance.
Catalog Number:
(89318-100)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to CAND2
Catalog Number:
(10494-030)
Supplier:
Bioss
Description:
Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The FAM80A gene product has been provisionally designated FAM80A pending further characterization.
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