2301 Results for: "Pyrrole-3-carboxylic+acid&pageNo=101&view=easy"

Supplier: VWR Collection

Simple one-key reset operation resets MIN/MAX memories.

Supplier: Cole Parmer

Compact, powerful, and programmable microcentrifuge.

Supplier: Avantor

Avantor® Hichrom RPB is a high purity base deactivated silica which offers a unique selectivity due to the proprietary C8/C18 multi-alkyl bonding and exhaustive endcapping employed. The range includes 3,5, 5 and 10 μm phases, which are suitable for LC-MS applications and preparative separations respectively.

Supplier: FRISTADS KANSAS

Overalls made from 65% polyester and 35% cotton, with soft nap on reverse side.

Supplier: FRISTADS KANSAS

These short trousers are made of 65% polyester and 35% cotton, with a soft nap on the reverse side. OEKO-TEX® certified.

Supplier: Avantor Fluid Handling

Make the most of your Masterflex flowmeters with these replacement parts and other accessories.

Supplier: FRISTADS KANSAS

These overalls with bib and braces are made from 65% polyester, 35% cotton, with a soft nap on reverse side.

Supplier: Thermo Fisher Scientific

Solaris incubated orbital shakers feature Peltier chillers, units have a compact footprint, are designed to fit on the benchtop, user programmability for easy setup and reproducibility plus connectivity for easy monitoring.

Supplier: SI Analytics

TitroLine® 7500 KF is a volumetric generalist for a wide range of uses. Applications include KF volumetry, dead-stop titrations (SO₂, bromine number), dosing tasks and preparation of solutions. Ideal for KF analysis in pharmaceutical, chemical, food and mineral oil industries.

Supplier: Brady

A rugged design offering seamless experience. Digitise data capture and automate your workflows with ease and accuracy with the V4500 Barcode Scanner.

Supplier: Hettich

High performance, compact centrifuges developed for high sample throughput as well as for high sample volumes.

Supplier: Thermo Fisher Scientific

Solaris incubated refrigerated orbital shakers feature Peltier chillers, units have a compact footprint, are designed to fit on the benchtop, user programmability for easy setup and reproducibility plus connectivity for easy monitoring.

Supplier: FRISTADS KANSAS

Overalls made from 65% polyester and 35% cotton, with soft nap on reverse side.

Supplier: ProSci Inc.

ATG101 Antibody: Autophagy, the process of bulk degradation of cellular proteins through an autophagosomic-lysosomal pathway is important for normal growth control and may be defective in tumor cells. It is involved in the preservation of cellular nutrients under starvation conditions as well as the normal turnover of cytosolic components. This process is negatively regulated by TOR (Target of rapamycin) through phosphorylation of autophagy protein ATG1. ATG101 is a recently discovered protein that stabilizes ATG13, another autophagy protein that forms a complex with the mammalian homologs of ATG1, ULK1 and ULK2, and with FIP200. This complex is a target of TOR phosphorylation under normal conditions; inhibition of TOR by rapamycin or leucine deprivation leads to dephosphorylation of ATG13, ULK1 and ULK2, which then leads to autophagy. ATG101 also interacts with ULK1 and is essential for autophagy.

Supplier: Bioss

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: Bioss

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: Bioss

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: Bioss

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: KIMBERLY CLARK

Kimberly-Clark Professional® Aquarius® black soap dispenser designed to be used with a range of Kleenex® and Scott® 1000 ml skincare cartridges.

Supplier: 3M

Secure Click™ P3 R D9035 hard case particulate filters are approved for use with 3M™ Secure Click™ respirators to provide protection against exposure to particles, dusts and mist in environments containing certain particles.

Supplier: JSP

EVO® VISTAlens® is a next generation, feature-rich safety helmet based on the proven Evolution® head protection technology. Incorporating a fully retractable optical class 1 integrated over spec. The eyewear is easy to deploy, adjust and maintain ensuring protection is on hand whenever it is required.

Supplier: Hettich

Powerful, compact bench top centrifuges with quiet and smooth running for processing microlitre tubes of 0,2 to 2,0 ml, used in clinical laboratories as well as in genetic research, virology and bacteriology.

Supplier: Hettich

Centrifuges with excellent performance and comprehensive range of accessories enabling them to carry out virtually any centrifuging task.

Supplier: OHAUS

Designed with energy efficiency in mind, the Compass CX series offers a battery life of up to 1000 continuous hours, allowing for uninterrupted operation. Compass™ CX scales have a stainless steel pan and are ideal for use in laboratory, industrial, education, and even household settings.

Supplier: Bioss

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: Bioss

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: Bioss

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: Essity

Tork PeakServe® Continuous™ paper hand towel dispenser black H5, high capacity, elevation range.

Supplier: OHAUS

Balances with multiple features, but uncomplicated weighing capabilities, provide the user with rapid, accurate results for routine weighing and measurement activities. Applications include weighing, formulation, check weighing and percentage weighing. Stabilisation times are typically less than three seconds.

Supplier: 3M

The G3000 helmet is made from UV-stabilised ABS and was designed in close collaboration with forestry, industrial and construction workers. It is intended for use in harsh environments with tough demands for effective protection, excellent ventilation and a maximum field of vision.