241665 Results for: "single-use assemblies"

Supplier: TriLink BioTechnologies

This nucleotide consists of an unmodified base, a ribose, and a 5′ triphosphate group for synthesis of RNA molecules.

Supplier: ANTIBODIES.COM

Mouse GM-CSF ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse GM-CSF in serum, plasma, and other biological fluids. This ELISA kit only requires 25 µl of sample volume(s).

Supplier: ANTIBODIES.COM

Mouse TIM 1 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse TIM 1 in serum, plasma, and other biological fluids. This ELISA kit only requires 25 µl of sample volume(s).

Supplier: ANTIBODIES.COM

Mouse RAGE ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse RAGE in serum, plasma, and other biological fluids. This ELISA kit only requires 25 µl of sample volume(s).

Supplier: VELP SCIENTIFIC

The OHS Series overhead stirrers are the ideal solution for the most demanding applications: The powerful brushless motor and microprocessor ensure excellent performance and make the VELP OHS Series overhead stirrers unlike any conventional stirrer.

Supplier: Merck

Sodium hydroxide 0.25 mol/l (0.25 N) in aqueous solution, Titripur® volumetric solution, Supelco®

Supplier: Merck

Iodine 0.05 mol/l (0.1 N) in aqueous solution, Titripur® Reag. Ph. Eur. volumetric solution, Supelco®

Supplier: Ansell

RINGERS^® R840 light-duty impact-resistant gloves feature a low profile level 1 TPR (Thermoplastic Rubber) impact technology providing optimal protection to the knuckles, thumb and full length of fingers.

Supplier: Brady

Securely label laboratory tubes and vials for cryogenic storage with this self-laminating, ultra-thin polyester label material (B-461). Print almost anywhere with a compact Brady portable label printer.

Supplier: IKA

Vortex mixer with three interchangeable attachments and various inserts for different applications. Microcentrifuge tubes, microtitre plates, even round bottomed or 250 ml Erlenmeyer flasks can be attached by means of the specially designed strap. Attachments click securely onto the unit in any position. The unit is stable at high speeds and sturdy with coated, zinc die-casting.

Supplier: Merck

Sodium hydroxide 2 mol/l (2 N) in aqueous solution, Titripur® volumetric solution, Supelco®

Supplier: Merck

Zinc, Certipur® Reag. Ph. Eur. volumetric standard, secondary reference material, for complexometry traceable to NIST, Supelco®

Supplier: Essity

Optimise consumption of the disposable cleaning cloths with the one-at-a-time dispensing feature. The Handy Box's large opening means cloths are easy to access, even when wearing gloves.

Supplier: DWK Life Sciences

Manufactured from 33 expansion, low extractable borosilicate glass. Thick uniform walls throughout and extra wall thickness built into the evenly tooled top rim.

Supplier: Thermo Fisher Scientific

Rapid-Flow™ disposable filter units with PES membrane, PS funnel and PP collection tube feature the exclusive Rapid-Flow support column design, providing fast flow rates and high throughput. The last line of defense against cell culture contamination and optimal choice for small volume tissue culture work. Offers clean, fast filtration of 20 to 50 ml of media or buffers.

Supplier: Bioss

FAM36A is a multi-pass membrane protein. It belongs to the FAM36 family. The exact function of FAM36A remains unknown.Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The FAM36A gene product has been provisionally designated FAM36A pending further characterization.

Supplier: Bioss

FAM36A is a multi-pass membrane protein. It belongs to the FAM36 family. The exact function of FAM36A remains unknown.Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The FAM36A gene product has been provisionally designated FAM36A pending further characterization.

Supplier: VWR Collection

Microscope slides with ground edges designed for human blood or fluid tests.

Supplier: VWR Collection

Insulated waterproof carrier.

Supplier: Bioss

FAM36A is a multi-pass membrane protein. It belongs to the FAM36 family. The exact function of FAM36A remains unknown.Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The FAM36A gene product has been provisionally designated FAM36A pending further characterization.

Supplier: Bioss

FAM36A is a multi-pass membrane protein. It belongs to the FAM36 family. The exact function of FAM36A remains unknown.Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The FAM36A gene product has been provisionally designated FAM36A pending further characterization.

Supplier: Bioss

FAM36A is a multi-pass membrane protein. It belongs to the FAM36 family. The exact function of FAM36A remains unknown.Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The FAM36A gene product has been provisionally designated FAM36A pending further characterization.

Supplier: Ansell

Mediumweight chemical-resistant gloves with excellent grip, dexterity and comfort. Silicone free.

Supplier: Bioss

FAM36A is a multi-pass membrane protein. It belongs to the FAM36 family. The exact function of FAM36A remains unknown.Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The FAM36A gene product has been provisionally designated FAM36A pending further characterization.

Supplier: VWR Collection

VWR® Nano Spectrophotometer is designed to simplify and accelerate your molecular biology research and routine applications.

Supplier: Avantor

Avantor® ACE® Excel® C18-PFP phase utilizes a specially developed ligand combining a C18 chain with integral PFP functionality. This results in a phase that maintains the hydrophobic, stability and low bleed characteristics of leading C18 phases, yet provides the multiple retention mechanisms of a PFP phase.

Supplier: Avantor

Everest columns have unique selectivity and sensitivity, which are the result of bonding technology that improves C18 surface coverage and deactivates residual silanols. Previously, the 300 Å C18 chemistries had carbon coverage in the 2,8 to 3,6 µmol/m² range. Everest C18 coverage is in excess of 4 µmol/m² and approximates the theoretical limit based on surface area. The increased shielding of the base silica increases column lifetime and reduces the amount of TFA required to shield the silica.

Supplier: PROTEXER

Shoe cover refill, BootieButler®, PE, Blue, Shoe size: U*

Supplier: MP Biomedicals

Metal bead lysing matrix contains 3,175 mm diameter stainless steel.

Supplier: GA

DYMO-compatible paper labels for printing with the DYMO 450-series of LabelWriter® printers.