16996 Results for: "2-Nitrobenzoyl+isocyanate&pageNo=16"

Supplier: Abnova

NCSTN RECOMBINANT PROTEIN (Q01) 1 * 1 EA

Supplier: Abnova

ROD1 RECOMBINANT PROTEIN (Q01) 1 * 1 EA

Supplier: Abnova

ELA3A RECOMBINANT PROTEIN (P01) 1 * 1 EA

Supplier: Portwest

Contemporary work trouser made from highly durable ripstop fabric that stretches as you move. Subtle articulation on the knees allow for increased freedom of movement and a high rise back waistband ensures protection in all working positions. Packed with functionality including pre-bent knees, a crotch gusset, two tier knee pad pockets and an adjustable leg length for added convenience.

Supplier: Thermo Fisher Scientific

This RO system with controller provides easy-to-read system parameters. Completely drainable, integrated 100 L high-purity water reservoir has a low-noise pressure booster as a standard component. The compact LabTower RO system is ideally suited as a feed water source for dishwashers, autoclaves and general laboratory use. It serves as a built-in pretreatment unit, consisting of a hardness stabilizer for protection of reverse osmosis module from hardness formers. An activated carbon/5 μm combi-cartridge protects the system against free chlorine and particles which ensures the long service life of downstream purification stages.

Supplier: UVP ULTRA VIOLET PRODUCTS

The innovative and compact design of the ColonyDoc-It™ enables automated, fast and accurate colony counting. The high resolution DSLR colour camera is specifically designed to capture white light and fluorescent marked colonies and a wide array of samples. The sophisticated yet intuitive system offers researchers easy detection and analysis of media. When colony samples require different light sources, the ColonyDoc-It™ enables the easy selection of bright LED lighting. The epi blue light and optional GFP filter enable users to visualise GFP fluorescence detection. The high resolution capabilities allow capture of images down to 0,8 mm. There is no need to adjust camera buttons, since the camera is easily controlled by the software. Connection to a PC/monitor (meeting a minimum specification) is required for full function.

Supplier: ProSci Inc.

Poly (ADP-ribosyl)ation is an immediate DNA-damage-dependent post-translational modification of histones and other nuclear proteins that contributes to the survival of injured proliferating cells. PARP16 is a member of poly (ADP-ribose) polymerases (PARPs) family that is encoded by different genes and displaying a conserved catalytic domain in which PARP-1 (113 kDa), the founding member, and PARP-2 (62 kDa) are so far the sole enzymes whose catalytic activity has been shown to be immediately stimulated by DNA strand breaks. A large repertoire of sequences encoding novel PARPs now extends considerably the field of poly (ADP-ribosyl)ation reactions to various aspects of the cell biology including cell proliferation and cell death. Some of these new members interact with each other, share common partners and common subcellular localizations suggesting possible fine tuning in the regulation of this post-translational modification of proteins.

Supplier: Agilent

HAYESEP A 80/10041.28MM COIL ULTIMETAL 1 * 1 ST

Supplier: VARIAN

[EN]O-RING SPRAY CHAMBER MARK 7 NITRILE 1 * 1 ST

Supplier: Pharmablock (USA)

TERT-BUTYL 3-BROMO-2-OXO-1,2,5,6,7,8-HEX 1 * 1 g

Supplier: WATERS

[EN]CORTECS C8 METHOD VALIDATION KIT, 90 1 * 3 ST

Supplier: witeg Labortechnik

[EN]DISPOSABLE CULTURE TUBES WITHOUT RIM 1 * 100 ST

Supplier: SCIENTIFIC INDUSTRIES ELMIS

Same great features of the Original Vortex-Genie® 2 in addition to programmability. These rugged and reliable vortex mixers have a durable motor, solid metal casing and rubber feet that prevent them 'walking'. The Vortex-Genie® Pulse is ideal for applications requiring more aggressive action than standard vortexing.

Supplier: Copan

Rapid DNA testing made portable. MicroFLOQ® is an innovative DNA collection tool featuring a micro flocked swab-head co-developed* by French Gendarmerie Forensic Research Institute (IRCGN™) and Copan.

Supplier: Bioss

The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma

Supplier: Bioss

The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma

Supplier: Bioss

The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

Supplier: Bioss

The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

Supplier: Bioss

The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma

Supplier: Bioss

The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma

Supplier: WATERS

[EN]CORTECS HILIC METHOD VALIDATION KIT, 1 * 3 ST

Supplier: WATERS

[EN]CORTECS C18+ METHOD VALIDATION KIT, 1 * 3 ST

Supplier: WATERS

[EN]CORTECS PHENYL METHOD VALIDATION KIT 1 * 3 ST

Supplier: Pharmablock (USA)

3-[2-[2-[[4-(2-AZATRICYCLO[10.4.0.0⁴⁹]HE 1 * 1 g

Supplier: WATERS

[EN]CORTECS HILIC METHOD VALIDATION KIT, 1 * 3 ST

Supplier: WATERS

[EN]CORTECS C18 METHOD VALIDATION KIT, 9 1 * 3 ST

Supplier: WATERS

[EN]CORTECS C8 METHOD VALIDATION KIT, 90 1 * 3 ST

Supplier: WATERS

[EN]CORTECS C8 METHOD VALIDATION KIT, 90 1 * 3 ST

Supplier: WATERS

[EN]CORTECS C8 METHOD VALIDATION KIT, 90 1 * 3 ST

Supplier: Pharmablock (USA)

6-TERT-BUTYL 1-ETHYL 6-AZASPIRO[2.5]OCTA 1 * 1 g