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Image Unavailable-PROOCIL-PCB-101-CS

Organic reference standard, 2,2',4,5,5'-Pentachlorobiphenyl (PCB No. 101) 100 µg/ml in isooctane, CIL

Description: Organic Standard, 2,2',4,5,5'-Pentachlorobiphenyl (PCB No. 101) 100 µg/ml in isooctane, Pack type: Glass bottle
Catalog Number: PROOCIL-PCB-101-CS
UOM: 1 * 1,2 mL
Supplier: LGC Standards PROMOCHEM
Image Unavailable-BOSSBS-9498R

Anti-C9orf153 Rabbit Polyclonal Antibody

Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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.
Catalog Number: BOSSBS-9498R
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-BOSSBS-9498R-CY5.5

Anti-C9ORF153 Rabbit Polyclonal Antibody (Cy5.5®)

Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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.
Catalog Number: BOSSBS-9498R-CY5.5
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-BOSSBS-9498R-CY3

Anti-C9ORF153 Rabbit Polyclonal Antibody (Cy3®)

Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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.
Catalog Number: BOSSBS-9498R-CY3
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-PRSI24-325

Anti-KCNJ13 Recombinant Antibody [Clone: SAIC-27C-101]

Description: Anti-KCNJ13 Recombinant Antibody [Clone: SAIC-27C-101]
Catalog Number: PRSI24-325
UOM: 1 * 0,2 mg
Supplier: ProSci Inc.

New Product


Image Unavailable-BOSSBS-9498R-HRP

Anti-C9ORF153 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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.
Catalog Number: BOSSBS-9498R-HRP
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-ANTIA86157-100

Anti-CD64 Mouse Monoclonal Antibody [clone: 10.1] (FITC (Fluorescein Isothiocyanate))

Description: Anti-CD64 Mouse Monoclonal Antibody [clone: 10.1] (FITC (Fluorescein Isothiocyanate))
Catalog Number: ANTIA86157-100
UOM: 1 * 100 T
Supplier: ANTIBODIES.COM

New Product


Image Unavailable-PRSI76-933

Anti-SDC1 Mouse Monoclonal Antibody [clone: DL-101] (PE (Phycoerythrin))

Description: The DL-101 monoclonal antibody specifically reacts with human CD138, a 85-92 kDa type I heparan sulfate proteoglycan. CD138 is known as Syndecan-1 and is expressed on pre-B cells, immature B cells, plasma cells, and malignant plasma cells, to the exclusion of mature circulating B cells. Syndecan-1 is also expressed on vascular smooth muscle, endothelial, neural, and embryonic mesenchymal cells. It is involved in cellular proliferation, cellular migration, and acts as an extracellular matrix receptor. Among the hematopoietic elements, CD138 is a useful marker for plasma cells.
Catalog Number: PRSI76-933
UOM: 1 * 100 Tests
Supplier: ProSci Inc.

New Product


Image Unavailable-ABNORAB03734.200UG

Anti-PCNA1 (Proliferating cellular nuclear antigen 1) conjugated to KLH Mouse Recombinant Antibody [clone: SAIC-27C-101]

Description: Anti-PCNA1 (Proliferating cellular nuclear antigen 1) conjugated to KLH Mouse Recombinant Antibody [clone: SAIC-27C-101]
Catalog Number: ABNORAB03734.200UG
UOM: 1 * 200 µG
Supplier: Abnova
Product Image-ROCK200-301-E57

Anti-IDO1 Mouse Monoclonal Antibody (Unconjugated) [clone: 10.1]

Description: Anti-IDO1 Mouse Monoclonal Antibody [clone: 10.1]
Catalog Number: ROCK200-301-E57
UOM: 1 * 100 µG
Supplier: Rockland Immunochemicals
Product Image-521-0301

Rotors for MR23i centrifuge

Description: Fixed angle rotor AM 100.13, 28°, 6×100 ml tubes (38×101 mm), 13000 min⁻¹, 18516×g, For: MR23i
Catalog Number: 521-0301
UOM: 1 * 1 items
Supplier: JOUAN
Product Image-353.

Staining jars

Description: PMP.
Catalog Number: 353.
UOM: 1 * 1 items
Supplier: KARTELL
Image Unavailable-ILMV402015

Accessories for standard duty diaphragm pumps, ILMVAC

Description: Service kit includes diaphragm, valves and O-rings, for MP/MPC 101 Z, 201 E
Catalog Number: ILMV402015
UOM: 1 * 1 items
Supplier: Welch by Gardner Denver
Product Image-ANTIA122022-100

Anti-CD64 Mouse Monoclonal Antibody [clone: 10.1] (PE-Cyanine 7)

Description: Mouse monoclonal [10.1] antibody to CD64 (PE-Cyanine 7) for Flow Cytometry with samples derived from human and Non-Human Primates.
Catalog Number: ANTIA122022-100
UOM: 1 * 100 T
Supplier: ANTIBODIES.COM

New Product


Image Unavailable-BOSSBS-9498R-FITC

Anti-C9ORF153 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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.
Catalog Number: BOSSBS-9498R-FITC
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-BOSSBS-9498R-A555

Anti-C9ORF153 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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.
Catalog Number: BOSSBS-9498R-A555
UOM: 1 * 100 µl
Supplier: Bioss
257 - 272 of 150 369