You Searched For: Lisinopril+dihydrate


10 258  results were found

Sort Results

List View Easy View
SearchResultCount:"10258"
Description: SupaTop syringe filters offer reliable and cost-effective solutions for particles removal and clarification needs.
Catalog Number: GILSANM1345D
UOM: 1 * 1.000 items
Supplier: GILSON


Description: Reusable clamps with PTFE-encapsulated steel spring core for connecting ground joint parts.
Catalog Number: BOHLH942-19
UOM: 1 * 1 items
Supplier: Bohlender


Description: Filters for sterilising or clarifying biological solutions. The larger filtration area increases flow rate and throughput. It also makes it easier to filter solutions because it reduces the pressure required to empty the syringe.
Catalog Number: SLVV033RS
UOM: 1 * 50 items
Supplier: Merck


Description: Needle, Gauge: 25, Length: 50 mm, Ø ext.: 0,50 mm, Type of tip: Side hole/dome, N25/500-5H
Catalog Number: 548-0990
UOM: 1 * 5 items
Supplier: Trajan Scientific and Medical


Description: Gemin7 is a 131 amino acid protein encoded by the mouse gene Gemin7. Gemin7, along with Gemin6, is a significant component of the the large multiprotein human SMN complex. The SMN complex functions as an assembly machine for small nuclear ribonucleoproteins (snRNPs)-the major components of the spliceosome. The survival of motor neurons (SMN) protein, a product of the disease gene of the common neurodegenerative disease, spinal muscular atrophy, is also part of the SMN complex. Although Gemin6 and Gemin7 have no significant sequence similarity with Sm proteins, both adopt canonical Sm folds. Moreover, Gemin6 and Gemin7 exist as a heterodimer, and interact with each other via an interface similar to that which mediates interactions among the Sm proteins. The Gemin6/Gemin7 complex binds to Sm proteins and might help organize Sm proteins for formation of Sm rings on snRNA targets.
Catalog Number: BOSSBS-13330R-CY3
UOM: 1 * 100 µl
Supplier: Bioss


Description: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of motor neurons in the spinal cord. SMA is caused by deletion or loss-of-function mutations in the SMN (Survival of Motor Neuron) gene. Gemin6, the protein product of human chromosome 2p22.2, associates directly with SMN and is a part of the SMN complex containing Gemin2, Gemin3, Gemin4 and Gemin5 as well as several spliceosomal snRNP proteins. The SMN complex plays an essential role in spliceosomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus. The SMN complex is found in both the cytoplasm and the nucleus. The nuclear form is concentrated in subnuclear bodies called gems (Gemini of the coiled bodies).
Catalog Number: BOSSBS-13333R-CY3
UOM: 1 * 100 µl
Supplier: Bioss


Description: G protein-coupled receptors (GPCRs) represent a large superfamily of cell-surface receptors that are involved in a multitude of physiological processes such as perception of sensory information, modulation of synaptic transmission, hormone release/actions, regulation of cell contraction/migration and cell growth/differentiation. GPCRs interact with G proteins (heterotrimeric GTPases) to synthesize intracellular second messengers, such as diacylglycerol, cyclic AMP, inositol phosphates and calcium ions. Their diverse biological functions range from vision and olfaction to neuronal and endocrine signaling and are involved in many pathological conditions. GRIN2 (G protein-regulated inducer of neurite outgrowth 2), also known as GPRIN2, is a 458 amino acid protein that is expressed in cerebellum and is thought to play a role in neurite outgrowth. GRIN2 interacts with activated G?oand G?, and is encoded by a gene that maps to human chromosome 10q11.22.
Catalog Number: BOSSBS-8276R-CY5
UOM: 1 * 100 µl
Supplier: Bioss


Description: Plastic syringe, 1 ml
Catalog Number: LOVI366110
UOM: 1 * 1 items
Supplier: Lovibond


Description: Accessory for density meter, Filling syringes, 5 ml
Catalog Number: BELL43-009
UOM: 1 * 1 items
Supplier: BELLINGHAM STANLEY


Description: Useful for prefiltration of particulate laden aqueous samples, serum filtration and dissolution testing.
Catalog Number: 516-1000
UOM: 1 * 200 items
Supplier: Cytiva (Formerly Pall Lab)

Environmentally Preferable


Description: Constructed from borosilicate glass, PTFE plunger tips and Kel-F® or PTFE Luer cones where applicable.
Catalog Number: 548-0935
UOM: 1 * 6 items
Supplier: Trajan Scientific and Medical


Description: Syringe, chromatography, HPLC, Gas-tight, with PTFE-tipped plunger, 1/4-28 UNF front thread, 250C-THERMOSPEC, Volume: 250 µl, For: AS100/300 and AS1000/3000/3500 LC autosamplers, Pk: 1
Catalog Number: 006660.
UOM: 1 * 1 items
Supplier: Trajan Scientific and Medical


Description: GPRIN1 may be involved in neurite outgrowth.
Catalog Number: BOSSBS-8275R-CY5
UOM: 1 * 100 µl
Supplier: Bioss


Description: Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of motor neurons in the spinal cord. SMA is caused by deletion or loss-of-function mutations in the SMN (Survival of Motor Neuron) gene. Gemin6, the protein product of human chromosome 2p22.2, associates directly with SMN and is a part of the SMN complex containing Gemin2, Gemin3, Gemin4 and Gemin5 as well as several spliceosomal snRNP proteins. The SMN complex plays an essential role in spliceosomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus. The SMN complex is found in both the cytoplasm and the nucleus. The nuclear form is concentrated in subnuclear bodies called gems (Gemini of the coiled bodies).
Catalog Number: BOSSBS-13333R-CY5
UOM: 1 * 100 µl
Supplier: Bioss


Description: Gemin4 is a component of the SMN core complex which, while in the cytoplasm, plays an essential role in ribonucleoprotein (snRNP) assembly, including the biogenesis, delivery and recycling of snRNPs to the spliceosome. In the nucleus, where SMN is required for pre-mRNA splicing, Gemin4 concentrates next to coiled bodies in subnuclear structures called gems, that are highly enriched in splicosomal snRNPs, and in the nucleolus. Deletion or loss-of-function mutations in the SMN lead to the neurodegenerative disease spinal muscular atrophy (SMA). The human Gemin4 maps to chromosome 17p13.
Catalog Number: BOSSBS-13328R-CY3
UOM: 1 * 100 µl
Supplier: Bioss


Description: Gemin4 is a component of the SMN core complex which, while in the cytoplasm, plays an essential role in ribonucleoprotein (snRNP) assembly, including the biogenesis, delivery and recycling of snRNPs to the spliceosome. In the nucleus, where SMN is required for pre-mRNA splicing, Gemin4 concentrates next to coiled bodies in subnuclear structures called gems, that are highly enriched in splicosomal snRNPs, and in the nucleolus. Deletion or loss-of-function mutations in the SMN lead to the neurodegenerative disease spinal muscular atrophy (SMA). The human Gemin4 maps to chromosome 17p13.
Catalog Number: BOSSBS-13328R-CY5
UOM: 1 * 100 µl
Supplier: Bioss


1 025 - 1 040 of 10 258