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Image Unavailable-75997-986

VWR® Screw Cap Erlenmeyer Flasks

Catalog Number: (75997-986)
Supplier: VWR International
Description: High-quality screw cap flasks featuring ASTM 438 standard and are a great value.

Certificates UL Listed


Image Unavailable-77984-091

TRC Erythromycin Estolate (>85%)

Catalog Number: (77984-091)
Supplier: LGC Standards
Description: TRC Erythromycin Estolate (>85%)

New Product


Image Unavailable-CAPX1000-3

Orthophosphoric acid ≥85-88% (w/w), Supelco®

Supplier: MilliporeSigma
Description: Orthophosphoric acid ≥85-88% (w/w), Supelco®

SDS Certificates

Product Image-59580-322

VWR® Solid Rubber Stoppers, Black

Catalog Number: (59580-322)
Supplier: VWR International
Description: These solid, black stoppers contain a high percentage of pure rubber, weigh less than neoprene, and are low in free sulfur (<sup>1</sup>/<sub>2</sub>%).
Image Unavailable-CAPIPA5-14651

Anti-FGFR2 Rabbit Polyclonal Antibody

Catalog Number: (CAPIPA5-14651)
Supplier: Thermo Scientific
Description: FGFR2 is a member of the fibroblast growth factor receptor family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This particular family member is a high-affinity receptor for acidic, basic and/or keratinocyte growth factor, depending on the isoform. Mutations in the gene are associated with many craniosynostotic syndromes and bone malformations. The genomic organization of the gene encompasses 20 exons. Alternative splicing in multiple exons, including those encoding the Ig-like domains, the transmembrane region and the carboxyl terminus, results in varied isoforms which differ in structure and specificity. Isoform 1 has equal affinity for aFGF and bFGF but does not bind KGF.
Image Unavailable-77992-614

TRC Ramipril Methyl Ester(>85%)

Catalog Number: (77992-614)
Supplier: LGC Standards
Description: TRC Ramipril Methyl Ester(>85%)

New Product


Image Unavailable-102882-434

Anti-BSG Mouse Monoclonal Antibody (Alexa Fluor® 700) [clone: TRA-1-85]

Catalog Number: (102882-434)
Supplier: R&D Systems
Description: Human TRA-1-85/CD147 Alexa Fluor 700, Monoclonal, Host: Mouse, Clone NO: TRA-1-85, Isotype: IgG1, Immunogen: 2120Ep human embryonal carcinoma cell line, Flow Cytometry
Image Unavailable-77976-236

TRC D-Glucono-1,4-lactone (>85%)

Catalog Number: (77976-236)
Supplier: LGC Standards
Description: TRC D-Glucono-1,4-lactone (>85%)

New Product


Image Unavailable-77992-010

TRC Potassium Hydroxide (~85%)

Catalog Number: (77992-010)
Supplier: LGC Standards
Description: TRC Potassium Hydroxide (~85%)

New Product


Image Unavailable-77985-739

TRC Alpha-Guaiene (>85%)

Supplier: LGC Standards
Description: TRC Alpha-Guaiene (>85%)

New Product

Image Unavailable-77989-356

TRC 2-Methyl-1-phenyl-1-propene (>85%)

Catalog Number: (77989-356)
Supplier: LGC Standards
Description: TRC 2-Methyl-1-phenyl-1-propene (>85%)

New Product


Image Unavailable-77992-714

TRC 9-cis,13-cis-Retinoic Acid, ~85%

Catalog Number: (77992-714)
Supplier: LGC Standards
Description: TRC 9-cis,13-cis-Retinoic Acid, ~85%

New Product


Image Unavailable-10494-046

Anti-RIMKLA Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (10494-046)
Supplier: Bioss
Description: 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 FAM80A gene product has been provisionally designated FAM80A pending further characterization.
Image Unavailable-10494-050

Anti-RIMKLA Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10494-050)
Supplier: Bioss
Description: 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 FAM80A gene product has been provisionally designated FAM80A pending further characterization.
Image Unavailable-10494-044

Anti-RIMKLA Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10494-044)
Supplier: Bioss
Description: 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 FAM80A gene product has been provisionally designated FAM80A pending further characterization.
Image Unavailable-10492-506

Anti-FAM78B Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10492-506)
Supplier: Bioss
Description: 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 FAM78B gene product has been provisionally designated FAM78B pending further characterization.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
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