97499 Results for: "N-Succinimidyl+trifluoroacetate&pageNo=25"

Supplier: SIGMA ALDRICH MICROSCOPY

Fluorinert™ belongs to the group of aliphatic compounds. It is considered as a pressure-transmitting medium because it is highly inert. Fluorinert™ Electronic Liquid FC-770 is a thermally stable, fully-fluorinated liquid that has ideal properties for use as a heat transfer fluid in a variety of industries. The inertness of Fluorinert™ FC-770 permits its use as a direct contact single and two-phase coolant in certain supercomputers and sensitive military electronics. Its high dielectric strength and electrical resistivity are ideal for applications in high voltage transformers and power electronics. In the semiconductor manufacturing industry, its wide liquid range makes Fluorinert™ liquid FC-770 suited for cooling ion implanters, dry etchers and CVD machines. Its low pour point also permits its use in thermal shock and test equipment.

Supplier: US Biological

LACTATE DEHYDROGENASE LD, LDHA PAB GT XR 1 * 100 µG

Supplier: TriLink BioTechnologies

CLEANCAP AG (3′ OME) CLEANSCRIPT IVT KIT 1 * 100 µl

Supplier: Merck

Titriplex® III ACS, ISO, Reag. Ph. Eur. analytical reagent, Supelco®

Supplier: US Biological

COE1 OLF, EBF FAMILY TRANSCRIP PAB RB XH 1 * 50 µG

Supplier: Tonbo Biosciences

APC-CYANINE7 ANTI-MOUSE CD5 (53-7.3) 1 * 100 G

Supplier: Tonbo Biosciences

APC-CYANINE7 ANTI-MOUSE CD69 (H1.2F3) 1 * 100 G

Supplier: Tonbo Biosciences

APC-CYANINE7 ANTI-MOUSE TER-119 TER-119 1 * 100 G

Supplier: Avantor

Ammonium iron(II) sulphate hexahydrate 98.5-101.5% (by KMnO₄ titration), fine crystals, BAKER ANALYZED® ACS, J.T.Baker®

Supplier: VWR Chemicals

EDTA disodium salt dihydrate BP, Ph. Eur., ACS, JP, USP

Supplier: Thermo Fisher Scientific

GeneJET Gel Extraction Kit is designed for rapid and efficient purification of DNA fragments from standard or low-melting point agarose gels run in either TAE or TBE buffer.

Supplier: VWR Chemicals

EDTA disodium salt dihydrate 99.0-101.0%, AnalaR NORMAPUR® ACS, Reag. Ph. Eur. analytical reagent

Supplier: Avantor Fluid Handling

Achieve high-accuracy multi-channel flow, with an intuitive touch-screen interface.

Supplier: VWR Collection

These anti-static coats are manufactured from 99% polyester fibres with 1% Hydro-Tec finish (carbon treated), which makes them both extremely durable and excellent for repelling dirt, oil, chemicals and water. All coats feature a stand-up collar, two side pockets and one breast pocket, all three protected by a flap.

Supplier: Avantor

J.T.Baker Robotic tips type TE MCA are compatible with the Tecan Freedom EVO and the Tecan Fluent liquid handler using the MCA 96 head. Tips are manufactured under automated processes to reduce human contact and ensure precise reproducibility and exceptional quality.

Supplier: LABCONCO

This filtered glove box with fibreglass liner provides inlet and outlet HEPA filtration and a leak-tight physical barrier to protect the operator from exposure to potentially hazardous materials. The glove box may also be appropriate for use as a containment isolator for applications that include compounds assigned ISO 4 and ISO 5 Banding Levels.

Supplier: LEICA MICROSYSTEMS

Leica DM750 microscopes have been specifically developed to facilitate science teaching. DM750 is designed essentially for the versatile needs of advanced life science courses and for professional training, such as in medical, veterinary and dental schools.

Supplier: Bioss

During development, genetically distinct subtypes of motor neurons express unique combinations of LIM-type homeodomain factors, which regulate cell migration and guide motor axons to establish the fidelity of a binary choice in axonal trajectory. The LIM gene family encodes a set of gene products, which carry the LIM domain, a unique cysteine-rich zinc-binding domain. At least 40 members of this family have been identified in vertebrates and invertebrates, and are distributed into 4 groups according to the number of LIM domains and to the presence of homeodomains and kinase domains. The human LHX5 gene maps to chromosome 12q23-q24 and encodes a 402 amino acid protein. The hippocampus contains the neural circuitry, which is crucial for cognitive functions such as learning and memory. LHX5 regulates precursor cell proliferation and neuronal differentiation and migration during hippocampal development.

Supplier: Bioss

CCDC25 is a 208 amino acid protein encoded by a gene that maps to human chromosome 8p21.1. 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: ENZO LIFE SCIENCES

Versatile tool for generation of ubiquitin-E2 thioesters.

Supplier: 3M

The 3M™ Aura™ Health Care Particulate Respirators provide effective respiratory protection for use in medical environments where health care workers will be exposed to airborne dust particles, non-volatile liquid particles and bioaerosols. These respirators limit the transmission of infective agents from staff to patients and are suitable for use during surgical procedures and certain other medical procedures. These products also offer resistance to penetration of splashes of liquid.

Supplier: BD Medical

PET, clear.

Supplier: Bioss

CCDC25 is a 208 amino acid protein encoded by a gene that maps to human chromosome 8p21.1. 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

CCDC25 is a 208 amino acid protein encoded by a gene that maps to human chromosome 8p21.1. 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: KLEINFELD

BOTTLE HEAVY DUTY SOLUTION KIMCOTE 1 * 1 items

Supplier: Thermo Fisher Scientific

Ammonium iron(II) sulphate hexahydrate ≥99.999% (metals basis), Puratronic®

Supplier: Bioss

CCDC25 is a 208 amino acid protein encoded by a gene that maps to human chromosome 8p21.1. 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

CCDC25 is a 208 amino acid protein encoded by a gene that maps to human chromosome 8p21.1. 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

GEFT is a 580 amino acid cytoplasmic protein that is highly expressed in excitable tissues such as brain, heart and muscle, and weakly expressed in small intestine, colon, liver, placenta and lung. GEFT may play a role in actin cytoskeleton reorganization in different tissues since its activation induces formation of actin stress fibers. GEFT works as a guanine nucleotide exchange factor for the Rho family of small GTPases and links specifically to G alpha q/11-coupled receptors in Rho A activation. GEFT is an important regulator of processes involved in axon and dendrite formation. Involved in skeletal myogenesis, GEFT seems to be an exchange factor primarily for Rac 1 in neurons. Existing as two alternatively spliced variants, GEFT contains a DH (DBL-homology) domain and a PH domain.

Supplier: Bioss

The protein encoded by this gene is a member of theTNF-receptor superfamily. This receptor is expressed preferentiallyin the tissues enriched in lymphocytes, and it may play a role inregulating lymphocyte homeostasis. This receptor has been shown tostimulate NF-kappa B activity and regulate cell apoptosis. Thesignal transduction of this receptor is mediated by various deathdomain containing adaptor proteins. Knockout studies in micesuggested the role of this gene in the removal of self-reactive Tcells in the thymus. Multiple alternatively spliced transcriptvariants of this gene encoding distinct isoforms have beenreported, most of which are potentially secreted molecules. Thealternative splicing of this gene in B and T cells encounters aprogrammed change upon T-cell activation, which predominantlyproduces full-length, membrane bound isoforms, and is thought to beinvolved in controlling lymphocyte proliferation induced by T-cellactivation. [provided by RefSeq, Jul 2008].