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SatPax® Polx® Pre-wetted, 100% Polyester Non-woven Cleanroom Wipes, Canister and Canister Refills

SatPax® Polx® Pre-wetted, 100% Polyester Non-woven Cleanroom Wipes, Canister and Canister Refills

Supplier: BERKSHIRE

SatPax® Polx® non-woven combines Polx non-woven wipers, composed of 100% polyester spunlace, with various saturation levels of isopropyl alcohol and DI water in an easy-to-dispense canister.

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HPLC columns, NUCLEODUR® C18 HTec

HPLC columns, NUCLEODUR® C18 HTec

Supplier: MACHEREY-NAGEL

NUCLEODUR® C18 HTec is a high density monomeric octadecyl modified silica phase for analytical and preparative HPLC.

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[EN]GASKET DOOR (IL 56PR PELTIER) 1 * 1 ST

Supplier: VWR Collection

[EN]GASKET DOOR (IL 56PR PELTIER) 1 * 1 ST

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WATER FOR INJECTION QUALITY WATER 200L 1 * 200 L

Supplier: Avantor

WATER FOR INJECTION QUALITY WATER 200L 1 * 200 L

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[EN]MS-CA 4/6 PUMP W/STEPPER 1 * 1 ST

Supplier: Avantor Fluid Handling

[EN]MS-CA 4/6 PUMP W/STEPPER 1 * 1 ST

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[EN]BRUSH SET 2/SET 1 * 1 ST

Supplier: Avantor Fluid Handling

[EN]BRUSH SET 2/SET 1 * 1 ST

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[EN]SU ASSY 1006317 1 * 1 ST

Supplier: Avantor Fluid Handling

[EN]SU ASSY 1006317 1 * 1 ST

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[EN]FLOWMETR TYPE 3360 2IN PVC EPDM 1 * 1 ST

Supplier: Avantor Fluid Handling

[EN]FLOWMETR TYPE 3360 2IN PVC EPDM 1 * 1 ST

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[EN]CABLE ADAPTER 24F 1 * 1 ST

Supplier: Avantor Fluid Handling

[EN]CABLE ADAPTER 24F 1 * 1 ST

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Anti-FAM91A1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Supplier: Bioss

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. The FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.

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Anti-FAM91A1 Rabbit Polyclonal Antibody (Cy5.5®)

Supplier: Bioss

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. The FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.

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Masterflex® B/T® modulaire digitale aandrijvingen, Avantor®

Masterflex® B/T® modulaire digitale aandrijvingen, Avantor®

Supplier: Avantor Fluid Handling

Overdracht en uitgifte van grote hoeveelheden.

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Anti-C9ORF91 Rabbit Polyclonal Antibody

Supplier: Bioss

Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf91 gene product has been provisionally designated C9orf91 pending further characterization. There are three isoforms of C9orf91 that are produced as a result of alternative splicing events.

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Trousers, Fristads® PR54-220, Design A, royal blue

Trousers, Fristads® PR54-220, Design A, royal blue

Supplier: FRISTADS KANSAS

Thanks to their durability and comfort, these trousers are perfectly suitable for use in garages as well as in industrial and service companies. The material is made of 65% polyester and 35% cotton. The inside is brushed and provides a comfortable cotton feel. The outside is very hardwearing and does not bleach, even after countless washes.

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Human LRP1 ELISA Kit

Human LRP1 ELISA Kit

Supplier: ANTIBODIES.COM

Human LRP1 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human LRP1 in serum, plasma, tissue homogenates, and other biological fluids.

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Membraanfilters Nuclepore™ met geëtste sporen, Whatman™

Membraanfilters Nuclepore™ met geëtste sporen, Whatman™

Supplier: Whatman products (Cytiva)

Nuclepore™ track-etched hydrophilic membrane filters offer a highly defined pore size cut-off in the submicron range, enabling particle deformity measurement and capture of extremely small particles. The membranes have sharply defined pores, high flow rates, and excellent chemical and thermal resistance. They are suitable for a variety of samples and applications, including microscopy, cytology, parasitology, and certain air and oceanography analyses.

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TSKgel® universal reversed phase columns

TSKgel® universal reversed phase columns

Supplier: TOSOH Bioscience

TSKgel ODS-100V/ODS-100Z columns incorporate the best-inclass surface properties to limit secondary interactions of basic, acidic and chelating compounds.

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Anti-FAM91A1 Rabbit Polyclonal Antibody

Supplier: Bioss

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. The FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.

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Anti-FAM91A1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Supplier: Bioss

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. The FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.

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Anti-FAM91A1 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Supplier: Bioss

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. The FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.

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Mouse LRP1 ELISA Kit

Mouse LRP1 ELISA Kit

Supplier: ANTIBODIES.COM

Mouse LRP1 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse LRP1 in serum, plasma, tissue homogenates, and other biological fluids.

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Anti-FAM91A1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Supplier: Bioss

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. The FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.

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Anti-FAM91A1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Supplier: Bioss

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. The FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.

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Micro-quartz fibre filters

Micro-quartz fibre filters

Supplier: Ahlstrom-Munksjö

Micro-quartz filters are useful for testing hot "stack" gases as the quartz fibers can withstand temperatures up to 900 °C. In addition, micro-quartz is used when the highest purity media is required. With excellent filtration properties and minimal traces of metals and minerals, quartz fibers are dimensionally stable and can be used in the analysis of acidic gases with the exception of hydrofluoric acid.

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Trousers, Fristads® PR54-220, Design B, Royal Blue

Trousers, Fristads® PR54-220, Design B, Royal Blue

Supplier: FRISTADS KANSAS

Thanks to their durability and comfort, these trousers are perfectly suitable for use in garages as well as in industrial and service companies. The material is made of 65% polyester and 35% cotton. The inside is brushed and provides a comfortable cotton feel. The outside is very hardwearing and does not bleach, even after countless washes.

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Rectangle Cryogenic Labels for Thermal Transfer Barcode Printers

Rectangle Cryogenic Labels for Thermal Transfer Barcode Printers

Supplier: GA

These labels are available in a range of sizes and configurations, perfect for identifying small diameter cryo vials, microtubes, cardboard or polypropylene cryo/freezer boxes, cell culture plates, and plastic bags.

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Anti-FAM91A1 Rabbit Polyclonal Antibody (Cy3®)

Supplier: Bioss

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. The FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.

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Anti-FAM91A1 Rabbit Polyclonal Antibody (Cy7®)

Supplier: Bioss

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. The FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.

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Anti-FAM91A1 Rabbit Polyclonal Antibody (Cy5®)

Supplier: Bioss

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. The FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.

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Overall, C.I., Design B, black

Supplier: FRISTADS KANSAS

Industrial overall made of 65% polyester and 35% cotton, with soft nap on reverse side. The black overall is available with several different accent colours. The accent colour can be found on the top of the collar, on the inside front flap, on the pocket edges and and as a stripe on front and back.

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