You Searched For: genome

Catalog Number: (BOSSBS-8076R-FITC)

Supplier: Bioss

Description: ARRDC1, ARRDC2 (which exists as multiple alternatively spliced isoforms), ARRDC4 and ARRDC5 are arrestin domain-containing proteins that are encoded by genes which map to human chromosomes 9, 15 and 19. Chromosome 9, on which the ARRDC1 gene is localised, contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. The ARRDC2 and ARRDC5 genes map to chromosome 19, which consists of over 63 million bases, houses approximately 1,400 genes and is recognised for having the greatest gene density of the human chromosomes. Unlike other ARRDC genes, the ARRDC4 gene maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localised genes.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-8076R-A680)

Supplier: Bioss

Description: ARRDC1, ARRDC2 (which exists as multiple alternatively spliced isoforms), ARRDC4 and ARRDC5 are arrestin domain-containing proteins that are encoded by genes which map to human chromosomes 9, 15 and 19. Chromosome 9, on which the ARRDC1 gene is localised, contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. The ARRDC2 and ARRDC5 genes map to chromosome 19, which consists of over 63 million bases, houses approximately 1,400 genes and is recognised for having the greatest gene density of the human chromosomes. Unlike other ARRDC genes, the ARRDC4 gene maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localised genes.

UOM: 1 * 100 µl

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Catalog Number: (USBIP9102-70L)

Supplier: US Biological

Description: Anti-Protein Gene Product 9.5 Rabbit Polyclonal Antibody

UOM: 1 * 100 µG

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Catalog Number: (USBIN2146-70E)

Supplier: US Biological

Description: Anti-Neuroepithelial Cell Transforming Gene 1 Goat Polyclonal Antibody

UOM: 1 * 100 µG

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Catalog Number: (USBIP9102-70G)

Supplier: US Biological

Description: Anti-Protein Gene Product 9.5 Rabbit Polyclonal Antibody

UOM: 1 * 50 µl

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Catalog Number: (USBII7662-94)

Supplier: US Biological

Description: Anti-Interferon Stimulating Gene 15 Rabbit Polyclonal Antibody

UOM: 1 * 500 µG

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Catalog Number: (USBIT8662-80)

Supplier: US Biological

Description: Anti-Trk-Fused Gene Protein Rabbit Polyclonal Antibody

UOM: 1 * 100 µG

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Catalog Number: (USBIC0115-02V)

Supplier: US Biological

Description: Anti-Calcitonin Gene-Related Peptide Rabbit Polyclonal Antibody

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-8024R-HRP)

Supplier: Bioss

Description: This gene belongs to the chemokine-like factor gene superfamily, a novel family that is similar to the chemokine and the transmembrane 4 superfamilies. This gene is one of several chemokine-like factor genes located in a cluster on chromosome 3. This gene is widely expressed in many tissues, but the exact function of the encoded protein is unknown. [provided by RefSeq, Jul 2008].

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-6394R-CY5.5)

Supplier: Bioss

Description: This gene encodes a protein that contains domains of thioredoxin and ERV1, members of two long-standing gene families. The gene expression is induced as fibroblasts begin to exit the proliferative cycle and enter quiescence, suggesting that this gene plays an important role in growth regulation. Two transcript variants encoding two different isoforms have been found for this gene.

UOM: 1 * 100 µl

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Catalog Number: (USBIN2915-52N-AP)

Supplier: US Biological

Description: Anti-N-myc Downstream Regulated Gene 1 Protein Rabbit Polyclonal Antibody (AP (Alkaline Phosphatase))

UOM: 1 * 200 µl

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Catalog Number: (ABCAAB208256-100)

Supplier: Abcam

Description: Alexa Fluor® 488 Rabbit monoclonal [EPR8766] to TRK fused gene.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-3309R-A750)

Supplier: Bioss

Description: This gene encodes a phosphoprotein which moves between the nucleus and the cytoplasm. The gene product is thought to be involved in several processes including regulation of the ARF/p53 pathway. A number of genes are fusion partners have been characterized, in particular the anaplastic lymphoma kinase gene on chromosome 2. Mutations in this gene are associated with acute myeloid leukemia. More than a dozen pseudogenes of this gene have been identified. Alternative splicing results in multiple transcript variants.

UOM: 1 * 100 µl

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Catalog Number: (USBIC1077-45)

Supplier: US Biological

Description: Anti-Capillary Morphogenesis Gene 2 Goat Polyclonal Antibody

UOM: 1 * 100 µG

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Catalog Number: (BOSSBS-6089R-CY3)

Supplier: Bioss

Description: This gene encodes a member of the Ras-assocation domain family (RASSF) of tumor suppressor proteins. This gene is essential for maintaining adherens junction function in epithelial cells and has a role in epithelial cell migration. It is a lung tumor suppressor gene candidate. A chromosomal translocation t(12;22)(p11.2;q13.3) leading to the fusion of this gene and the FBLN1 gene is found in a complex type of synpolydactyly. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-6089R-CY5.5)

Supplier: Bioss

Description: This gene encodes a member of the Ras-assocation domain family (RASSF) of tumor suppressor proteins. This gene is essential for maintaining adherens junction function in epithelial cells and has a role in epithelial cell migration. It is a lung tumor suppressor gene candidate. A chromosomal translocation t(12;22)(p11.2;q13.3) leading to the fusion of this gene and the FBLN1 gene is found in a complex type of synpolydactyly. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.

UOM: 1 * 100 µl

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