9079 Results for: "2-Bromo-4,5-difluorotoluene"
Anti-C19ORF45 Rabbit Polyclonal Antibody (Cy7®)
Supplier: Bioss
C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Expand 1 Items
SP Bel-Art Adjustable Microplate Tilting Stand, Bel-Art Products, a part of SP
Supplier: Bel-Art Products, a Part of SP
Make precise additions of liquid components to microplate wells by adjusting plates to the most convenient angle.
Expand 1 Items
Temp+rh Module for High-Precision Monitoring with Rapid Response Time
Supplier: SENSEANYWHERE BV
The SenseAnywhere Temp+rh Module offers precise temperature and humidity monitoring from −40 to +70 °C and 0 to 99% rh (non-condensing) with swift response time.
Expand 1 Items
![313376_260x190.jpg](https://occapi.avantorsciences.com/medias/313376-260x190.jpg?context=bWFzdGVyfGltYWdlc3w5NDQ1fGltYWdlL2pwZWd8YURReUwyZzFZUzg1TnpBMk1ETTBOekkwT0RrMEx6TXhNek0zTmw4eU5qQjRNVGt3TG1wd1p3fGY0MjhiMmY1ZGJjNTY3NDdlZDk5ZjMwMGEyYTdmYjNkY2IyNWE2ZmI1MTg2YTM4MjE0MTY4MmNiYjVmNTViMTE)
Now Available: Our latest edition of elements!
Unlock innovation! Packed with products from both our leading suppliers and our exclusive Avantor® brands.
Motic SMZ-171-TLED Trinocular Stereo Microscopes with Moticam, Camera Bundle
Supplier: Motic
With the new SMZ-171 Stereo Zoom microscope Motic proudly introduces an optically improved addition to its well-established SMZ Stereo series. New materials for ESD compatibility as well as optimized LED illumination options have been added to this series to create a versatile Stereo microscope platform for a wide range of biological and material science applications.
Expand 1 Items
XPert™ Bulk Powder Filtered Systems, Labconco®
Supplier: Labconco
Bulk powder systems keep airborne particulates and fumes contained during powder transfer procedures
Expand 12 Items
VWR® Signature™ Forced Air Safety Ovens
Supplier: VWR International
These microprocessor-controlled forced air units are equipped with a blow-out back panel to protect the user from injury.
Expand 1 Items
VWR® Routine LED Zoom Stereo Series
Supplier: VWR International
VWR® Routine LED Zoom Stereo Binocular microscope is ideal for educational environments and routine industrial applications. It’s Greenough optical system gives it a high degree of longevity, making it perfect for consistent, repetitive use, and its compact design means it will fit nicely in a classroom setting.
Expand 2 Items
CENCO® Quantitative Centripetal Force Apparatus
Supplier: Wards
The Quantitative Centripetal Force Apparatus' simple concept and robust construction guarantee reliable lab success.
Expand 2 Items
Glass Plates, Cytiva
Supplier: Cytiva
The key to reproducible electrophoresis results is temperature control. Gels cooled on their two faces produce slanted bands appearing as broad or double bands in stained gels. SE 600 Ruby ensures uniform heat in gels because, the gels are immersed in the lower buffer for uniform heat transfer and a standard magnetic stirrer circulates buffer around the vertically suspended heat exchanger to maintain homogeneous lower buffer temperature. The ergonomic SE 600 Ruby provides two built-in side handles, which facilitates carrying and handling. Run up to four gels (up to 112 samples) in a single run. Divider plates convert single-gel sandwiches into two-gel club sandwiches, which seal and fit into the casting stand like single gels. If gels longer than 16-cm are required, Cytiva offers the SE 660, which runs gels up to 24 cm. Except for gel lengt, the SE 660 has identical features to those of SE 600 Ruby.
Expand 1 Items
Anti-C19ORF45 Rabbit Polyclonal Antibody (Alexa Fluor® 350)
Supplier: Bioss
C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Expand 1 Items
Anti-C19ORF45 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Supplier: Bioss
C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Expand 1 Items
Anti-C19ORF45 Rabbit Polyclonal Antibody (Cy3®)
Supplier: Bioss
C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Expand 1 Items
Motic AE2000 Trinocular Inverted Microscope with Moticam, Camera Bundle
Supplier: Motic
Designed for routine-lab or clinical work, as well as research requirements in pharmaceutical laboratories or universities, the AE2000 is more than capable of fulfilling the expectations of its users. Superb optical quality can be expected from a brand new optical series of both bright field and phase contrast lenses, following Motic ́s proven successful CCIS® Infinity Optical System.
Expand 1 Items
Anti-C19ORF45 Rabbit Polyclonal Antibody (Cy5®)
Supplier: Bioss
C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Expand 1 Items
Anti-C19orf45 Rabbit Polyclonal Antibody
Supplier: Bioss
C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Expand 1 Items
Anti-C19ORF45 Rabbit Polyclonal Antibody (Alexa Fluor® 488)
Supplier: Bioss
C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Expand 1 Items
Anti-C19ORF45 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
Supplier: Bioss
C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Expand 1 Items
Anti-SERPINE1 Rabbit Polyclonal Antibody
Supplier: Prosci
PAI1 (plasminogen activator inhibitor 1) is originally cloned from human endothelial cell (Pannekoek 1986, Ginsburg 1986) and rat hepatoma cell 3 cDNA libraries. As a member of the serpin family of serine protease inhibitors, PAI1 inhibits both tissue type palsminogen activator (tPA) and urokinase type plasminogen activator (uPA). High PAI1 levels are associated with an increased risk of thromboembolic disease while PAI1 deficiency may represent an inherited autosomal recessive bleeding disorder.
Expand 1 Items
PIG® High-Visibility Safety Floor Runners, New Pig
Supplier: New Pig
Provide a no-slip path in hazardous walking areas with this super-safe, adhesive-backed absorbent runner — its hi-viz yellow safety edges can't be missed.
Expand 3 Items
Base Stands and Accessories for Purifier® Logic® Series Class II Safety Cabinets, Labconco®
Supplier: Labconco
Logic Cart fits under any telescoping base stand. Features three small and one large compartments, one drawer, front panel cut out for dispensing wipers or gloves, and HDPE worksurface. W×D×H: 635×483×686 mm (25×19×27").
Expand 52 Items
Anti-C19ORF45 Rabbit Polyclonal Antibody (Alexa Fluor® 647)
Supplier: Bioss
C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Expand 1 Items
Glassware washer accessories, FlaskScrubber® and SteamScrubber®
Supplier: Labconco
There is a wide selection of accessories to customize your glassware washer to your specific needs and applications. These racks and accessories are for use with Labconco FlaskScrubber®, SteamScrubber®, FlaskScrubber® Vantage glassware washers. Racks and inserts are stainless steel unless otherwise stated.
Expand 47 Items
Anti-C19ORF45 Rabbit Polyclonal Antibody (Cy5.5®)
Supplier: Bioss
C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Expand 1 Items
Anti-C19ORF45 Rabbit Polyclonal Antibody (Alexa Fluor® 555)
Supplier: Bioss
C19orf45 is a 505 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Expand 1 Items
Celestron Starsense Explorer Telescope, 114 mm
Supplier: Celestron International
This 114 mm aperture Celestron StarSense explorer telescope is ideal for beginners, thanks to the app's user-friendly interface and detailed tutorials.
Expand 1 Items
Anti-CFAP45 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
Supplier: Bioss
CCDC19 is a 466 amino acid protein encoded by a gene mapping to human chromosome 1. 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, Parkinson’s, 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.
Expand 1 Items
Anti-CFAP45 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Supplier: Bioss
CCDC19 is a 466 amino acid protein encoded by a gene mapping to human chromosome 1. 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, Parkinson’s, 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.
Expand 1 Items
qScript™ 1-Step Virus ToughMix®, Virus Detection Kit, Quantabio
Supplier: Quantabio
Superior sensitivity for viral RNA detection.
Expand 6 Items
Anti-CFAP45 Rabbit Polyclonal Antibody (Alexa Fluor® 647)
Supplier: Bioss
CCDC19 is a 466 amino acid protein encoded by a gene mapping to human chromosome 1. 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, Parkinson’s, 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.
Expand 1 Items
Protector® ClassMate™ Laboratory Hoods, Labconco®
Supplier: Labconco
ClassMate™ laboratory hoods are designed to meet the needs of instructional laboratories.