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chromatography+columns+HyClone+products+(Cytiva)
Catalog Number:
(10495-996)
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:
(10494-618)
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.
Supplier:
Restek
Description:
Use of these liners helps ensure an inert GC flow path for higher sensitivity, accuracy, and reproducibility.
Supplier:
HARDY DIAGNOSTICS CA
Description:
CRITERION™ Selenite Cystine Broth is for selective cultivation of <i>Salmonella spp.</i> from food, feces, dairy products and other sanitary materials
Supplier:
Restek
Description:
SGE syringes are designed and tested to meet critical autosampler performance needs.
Catalog Number:
(89085-134)
Supplier:
Ampac Flexibles
Description:
Ampac's FoilPAK (Non-Autoclave) pouches provide the best oxygen and moisture barrier available.
Catalog Number:
(89204-898)
Supplier:
Qorpak
Description:
Natural HDPE modern round bottles feature side panels to allow for label application.
Catalog Number:
(10374-212)
Supplier:
Bioss
Description:
Mutations in this gene lead to tuberous sclerosis complex. Its gene product is believed to be a tumor suppressor and is able to stimulate specific GTPases. The protein associates with hamartin in a cytosolic complex, possibly acting as a chaperone for hamartin. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq].
Catalog Number:
(10390-090)
Supplier:
Bioss
Description:
This gene encodes a membrane-bound adenylate cyclase that catalyses the formation of cyclic AMP from ATP and is inhibitable by calcium. The product of this gene is a member of the adenylyl cyclase class-4/guanylyl cyclase enzyme family that is characterized by the presence of twelve membrane-spanning domains in its sequences. [provided by RefSeq, Jul 2008].
Catalog Number:
(CA10063-922)
Supplier:
LONZA PHARMA - BIOSCIENCE CA
Description:
Bovine Pituitary Extract is useful in the culture of various epithelial cell types. The product is included in SingleQuots® Kits associated with various media systems for epithelial cell types. The product is available at a concentration of 13 mg/ml.
Catalog Number:
(CAMB-057)
Supplier:
Rockland Immunochemical
Description:
This product is ready-to-use as a working 1X solution and requires no further dilution
Supplier:
NATIONAL SCIENTIFIC COMPANY
Description:
Use Thermo Scientific™ SureSTART™ glass crimp top headspace vials, performance level 3, for your volatile gas analyzes.
Catalog Number:
(76338-136)
Supplier:
Marlin Steel Wire Products
Description:
Rugged material handling basketand dividers to constain small parts in pockets.
Catalog Number:
(10853-524)
Supplier:
Restek
Catalog Number:
(10479-780)
Supplier:
Bioss
Description:
Encoding over 1,100 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 FAM101A gene product has been provisionally designated FAM101A pending further characterization.
Supplier:
Encon Safety Products
Description:
This combination shower/face and eye wash with bowl is made with schedule 80 hot dip galvanized steel piping.
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