You Searched For: Tyrphostin+AG+1024

Catalog Number: (BOSSBS-3872R-A488)

Supplier: Bioss

Description: Transcriptional activator or repressor which probably serves as a general switch factor for erythroid development. It binds to DNA sites with the consensus sequence 5'-[AT]GATA[AG]-3' within regulatory regions of globin genes and of other genes expressed in erythroid cells.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-5890R-A350)

Supplier: Bioss

Description: Present in the extracellular matrix of human articular cartilage at all ages, although its abundance is far greater in the adult. In the adult cartilage lumican exists predominantly in a glycoprotein form lacking keratan sulfate, whereas the juvenile form of the molecule is a proteoglycan.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-5890R-A750)

Supplier: Bioss

Description: Present in the extracellular matrix of human articular cartilage at all ages, although its abundance is far greater in the adult. In the adult cartilage lumican exists predominantly in a glycoprotein form lacking keratan sulfate, whereas the juvenile form of the molecule is a proteoglycan.

UOM: 1 * 100 µl

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Supplier: SCHOTT AG Lighting and imaging

Description: TLS adapter Ø = 84 for base plate Ø 100 mm

Supplier: SCHOTT AG Lighting and imaging

Description: Cold light source, Holder for focusing lens (631-0009)

Catalog Number: (ENZOBMLG1400050)

Supplier: ENZO LIFE SCIENCES

Description: <i>Clostridium difficile</i> toxin A from <i>Clostridium difficile</i>, strain VPI10463 is a high potency toxin applicable to ELISA, antibody capture, cytotoxicity studies and LINE assay.

UOM: 1 * 50 µG

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Catalog Number: (BOSSBS-11004R)

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 FAM63A gene product has been provisionally designated FAM63A pending further characterization.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-15057R)

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 C1orf21 gene product has been provisionally designated C1orf21 pending further characterization.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-8230R)

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 FAM102B gene product has been provisionally designated FAM102B pending further characterization.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-3872R-CY5)

Supplier: Bioss

Description: Transcriptional activator or repressor which probably serves as a general switch factor for erythroid development. It binds to DNA sites with the consensus sequence 5'-[AT]GATA[AG]-3' within regulatory regions of globin genes and of other genes expressed in erythroid cells.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-5890R-CY5)

Supplier: Bioss

Description: Present in the extracellular matrix of human articular cartilage at all ages, although its abundance is far greater in the adult. In the adult cartilage lumican exists predominantly in a glycoprotein form lacking keratan sulfate, whereas the juvenile form of the molecule is a proteoglycan.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-5890R-CY5.5)

Supplier: Bioss

Description: Present in the extracellular matrix of human articular cartilage at all ages, although its abundance is far greater in the adult. In the adult cartilage lumican exists predominantly in a glycoprotein form lacking keratan sulfate, whereas the juvenile form of the molecule is a proteoglycan.

UOM: 1 * 100 µl

Sale

Catalog Number: (ENZOBMLG1500050)

Supplier: ENZO LIFE SCIENCES

Description: <i>Clostridium difficile </i>toxin B from<i> Clostridium difficile</i>, strain VPI10463 is a high purity toxin applicable to ELISA, antibody capture, cytotoxicity studies and LINE assay.

UOM: 1 * 50 µG

Sale

Catalog Number: (BOSSBS-3872R-A350)

Supplier: Bioss

Description: Transcriptional activator or repressor which probably serves as a general switch factor for erythroid development. It binds to DNA sites with the consensus sequence 5'-[AT]GATA[AG]-3' within regulatory regions of globin genes and of other genes expressed in erythroid cells.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-5890R-HRP)

Supplier: Bioss

Description: Present in the extracellular matrix of human articular cartilage at all ages, although its abundance is far greater in the adult. In the adult cartilage lumican exists predominantly in a glycoprotein form lacking keratan sulfate, whereas the juvenile form of the molecule is a proteoglycan.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-4890R-CY7)

Supplier: Bioss

Description: Modulates B-cell activation responses. Signaling could be triggered by the binding of a lectin-like ligand to the CD24 carbohydrates, and transduced by the release of second messengers derived from the GPI-anchor. Promotes AG-dependent proliferation of B-cells, and prevents their terminal differentiation into antibody-forming cells.

UOM: 1 * 100 µl

Sale