10116 Results for: "3-Fluoro-5-(trifluoromethyl)benzyl+bromide&pageNo=19"

Supplier: MOLNLYCKE HEALTH CARE

These natural rubber latex gloves provide an excellent barrier in general surgical procedures. The unique Biogel® hydrogel polymer coating on the inner surface makes them easy to don, even with damp hands. The coating also soothes the skin to help prevent moisture loss.

Supplier: MICRONOVA

The Isolator Tool™ adapter with a 360° swivel works with a range of mop covers to efficiently clean and disinfect isolators, hoods, RABS, and small equipment in clean and aseptic areas.

Supplier: FRISTADS KANSAS

Work trousers made from 65% polyester and 35% cotton, in a luxury fabric. With rubber-free, elastic straps and adjustable waist.

Supplier: Ahlstrom-Munksjö

Ahlstrom-Munksjö’s qualitative grades of filter paper are recommended for use in analytical methods which determine or identify particulate constituents of a mixture irrespective of the amount present. Qualitative filter papers are often used in routine separation work that still requires high purity and consistent performance. These filter papers covers a wide range of laboratory applications, as liquids clarification, qualitative analytical separations for precipitates and buffers filtration, and are also used for soil analysis and in food and beverage testing. Standard qualitative filter papers are suitable for quadrant folded or gravity flow applications.

Supplier: TOSOH BIOSCIENCE

SkillPak™ BIO pre-packed columns are designed for a fast method development and scale-up of multi-column chromatography (MCC) or continuous chromatography processes. They are pre-packed with TOYOPEARL® process chromatography media for bioseparations.

Supplier: Antibodies.com

Human SLC19A3 ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human SLC19A3 in serum, plasma, and other biological fluids.

Supplier: ProSci Inc.

TBX19 is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. TBX19 is the human ortholog of mouse Tbx19/Tpit gene. Studies in mouse show that Tpit protein is present only in the two pituitary pro-opiomelanocortin (POMC)-expressing lineages, the corticotrophs and melanotrophs. Mutations in the human ortholog were found in patients with isolated deficiency of pituitary POMC-derived ACTH, suggesting an essential role for this gene in differentiation of the pituitary POMC lineage.

Supplier: MACHEREY-NAGEL

NUCLEODUR® C18 ec is a medium density monomeric octadecyl modified silica phase for HPLC.

Supplier: SIOEN

Protective, single colour jacket made of 100% soft double-sided polyester fleece providing good cold protection. With anti-pilling treatment and stitched seams.

Supplier: Whatman products (Cytiva)

Whatman Puradisc syringe filters from Cytiva's business combine premium quality with economic efficiency. They are well suited for rapid, routine syringe filtration of samples up to 100 ml.

Supplier: MICROSOLV

Cogent TYPE-C Silica™ is HPLC grade silica with a silica hydride surface. Their unique stationary phase will adsorb and desorb solvents commonly used in mobile phases very differently from ordinary silica resulting in excellent benefits to the chromatographer. Excellent for normal phase chromatography and solvent drying is not needed.

Supplier: Bioss

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.

Supplier: Brand

The PD-Tips II dispenser tips for efficient, step-by-step dispensing enhance the proven features of the classic BRAND PD-Tips. Thanks to patented size coding, HandyStep® touch and HandyStep® electronic automatically detect the tip volume. The tips are also compatible with all other instruments of the HandyStep® family and with repetitive pipettes from other manufacturers.

Supplier: bimos

Neon supports the forward leaning sitting position that is often necessary in lab work. Its modern design matches the high-tech laboratory environment perfectly and has all the characteristics you would expect of a good laboratory chair. It is seamless, easy to clean, washable, and resistant to disinfectants making Neon the ideal solution for the laboratory when a really comfortable ergonomic chair is needed.

Supplier: Bioss

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.

Supplier: Biotium

This is a highly cross-adsorbed goat anti-mouse IgG (H L) secondary antibody labeled with our bright and photostable CF® Dyes. To minimise cross-reactivity, the antibody has been adsorbed against bovine, horse, human, rabbit, and swine serum. This antibody is not cross-adsorbed against rat. For staining rat tissue, or co-staining with rat antibodies, we recommend using Goat Anti-Mouse IgG (H L), Highly Cross-Adsorbed (Min x Rat).

Supplier: Bioss

CCDC12, also known as FLJ39430, FLJ40801 or MGC23918, is a 166 amino acid protein encoded by a gene mapping to human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

Supplier: asecos

Fireproof safety cabinets, classified type 30 (fire resistant up to 30 minutes), safe, durable, robust and convenient with transport base and bicoloured cabinet design.

Supplier: HELLMA

Hellma® high precision quartz glass flow-through cells for absorption measurements in the UV/Vis range and/or fluorescence measurements, 0,1 to 50 mm path length, with inlet and outlet nozzle, or 2 screw connections and FEP tubes.

Supplier: Testo

The testo 883 thermal imager provides outstanding image quality, automatic allocation/archiving of thermal images to the measurement object and professional image analysis and reporting.

Supplier: BD Medical

These EDTA tubes are used to obtain a whole blood or EDTA plasma sample.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

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.

Supplier: Bioss

CCDC12, also known as FLJ39430, FLJ40801 or MGC23918, is a 166 amino acid protein encoded by a gene mapping to human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

Supplier: Thermo Fisher Scientific

ClipTip™ pipette tips provide security with a unique and innovative interlocking technology that ensures a complete seal on every channel with minimal tip attachment and ejection force.

Supplier: ALSICO HIGHTECH

These cleanroom coveralls are made of Alsistrong® (98% polyester and 2% carbon). Suitable for the highest cleanroom classes ISO 4 to 9 or GMP classes A to D.

Supplier: FRISTADS KANSAS

Working trousers made of FAS®, Fristads best navy twill manufactured from 100% cotton.

Supplier: MACHEREY-NAGEL

NUCLEODUR® C18 Isis is a specially crosslinked octadecyl modified silica phase for HPLC with multi-endcapping.

Supplier: Antibodies.com

Human GALK1 ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human GALK1 in serum, plasma, and other biological fluids.