Du Søgte efter: genome

Varenummer: (BOSSBS-8498R-CY5.5)

Leverandør: Bioss

Beskrivelse: REG1 beta is a type I subclass member of the Reg gene family. The Reg gene family is a multigene family grouped into four subclasses, types I, II, III and IV based on the primary structures of the encoded proteins. REG1 beta highly similar to the REG1 alpha protein. The related REG1 alpha protein is associated with islet cell regeneration and diabetogenesis, and may be involved in pancreatic lithogenesis. Reg family members REG1 alpha, REGL, PAP and this gene are tandomly clustered on chromosome 2p12 and may have arisen from the same ancestral gene by gene duplication.

UOM: 1 * 100 µl

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Varenummer: (BOSSBS-4219R-FITC)

Leverandør: Bioss

Beskrivelse: The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This encoded protein is found as a subunit in corepressor SMRT (silencing mediator for retinoid and thyroid receptors) complex along with histone deacetylase 3 protein. This gene is located adjacent to the ocular albinism gene and it is thought to be involved in the pathogenesis of the ocular albinism with late-onset sensorineural deafness phenotype. Four transcript variants encoding two different isoforms have been found for this gene. This gene is highly similar to the Y chromosome TBL1Y gene. [provided by RefSeq].

UOM: 1 * 100 µl

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Varenummer: (BOSSBS-11282R)

Leverandør: Bioss

Beskrivelse: EVC is an autosomal skeletal dysplasia caused by mutations in the EVC and EVC2 genes. Found in developing ribs, heart, kidney and lung, the EVC gene is responsible for normal development of the face, limbs, teeth and nails. The protein expressed by the EVC gene is an intracellular component of the hedgehog signal pathway that contains a leucine zipper and transmembrane domain. Defects in the EVC gene can lead to short-limb dwarfism, ectodermal dysplasia and cardiac anomalies such as irregular atrioventricular septum development. Additionally, the EVC gene has been implicated in Weyers acrodental dysostosis, an autosomal dominant disease characterized by facial abnormalities and limb defects.

UOM: 1 * 100 µl

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Varenummer: (USBIC0115-01C-100)

Leverandør: US Biological

Beskrivelse: Anti-Calcitonin Gene Related Peptide Mouse Monoclonal Antibody [clone: 2Q2268]

UOM: 1 * 1 Each

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Varenummer: (USBIP9102-70D-250)

Leverandør: US Biological

Beskrivelse: Anti-Protein Gene Product 9.5 Mouse Monoclonal Antibody [clone: 5G201]

UOM: 1 * 250 µl

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Varenummer: (BOSSBS-9484R)

Leverandør: Bioss

Beskrivelse: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The LOC285636 gene product has been provisionally designated LOC285636 pending further characterization.

UOM: 1 * 100 µl

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Varenummer: (BSENR-1621-100)

Leverandør: Biosensis

Beskrivelse: This gene encodes an enzyme which catalyzes the biosynthesis of the neurotransmitter acetylcholine. This gene product is a characteristic feature of cholinergic neurons, and changes in these neurons may explain some of the symptoms of Alzheimer's disease. Polymorphisms in this gene have been associated with Alzheimer's disease and mild cognitive impairment. Mutations in this gene are associated with congenital myasthenic syndrome associated with episodic apnea. Multiple transcript variants encoding different isoforms have been found for this gene, and some of these variants have been shown to encode more than one isoform. [provided by RefSeq, May 2010]

UOM: 1 * 1 Each

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Varenummer: (USBIP9102-70K-100)

Leverandør: US Biological

Beskrivelse: Anti-Protein Gene Product 9.5 Mouse Monoclonal Antibody [clone: 8k263]

UOM: 1 * 100 µl

Tilbud

Varenummer: (USBIP9102-71J)

Leverandør: US Biological

Beskrivelse: Anti-Protein Gene Product 9.5 Mouse Monoclonal Antibody [clone: 9L605]

UOM: 1 * 1 Each

Tilbud

Varenummer: (USBIC0115-03-100)

Leverandør: US Biological

Beskrivelse: Anti-Calcitonin-Gene related Peptide 2 Goat Polyclonal Antibody

UOM: 1 * 100 µl

Tilbud

Varenummer: (USBI138591-100)

Leverandør: US Biological

Beskrivelse: Anti-Protein Gene Product 9.5 Mouse Monoclonal Antibody [clone: 31A3]

UOM: 1 * 1 Each

Tilbud

Varenummer: (BOSSBS-15444R-A647)

Leverandør: Bioss

Beskrivelse: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-15444R-A750)

Leverandør: Bioss

Beskrivelse: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4 kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-15208R)

Leverandør: Bioss

Beskrivelse: C5orf49 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf49 gene product has been provisionally designated C5orf49 pending further characterization.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-15206R)

Leverandør: Bioss

Beskrivelse: C5orf45 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf45 gene product has been provisionally designated C5orf45 pending further characterization.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-3303R-A750)

Leverandør: Bioss

Beskrivelse: This gene encodes a cell surface tyrosine kinase receptor for members of the platelet-derived growth factor family. These growth factors are mitogens for cells of mesenchymal origin. The identity of the growth factor bound to a receptor monomer determines whether the functional receptor is a homodimer or a heterodimer, composed of both platelet-derived growth factor receptor alpha and beta polypeptides. This gene is flanked on chromosome 5 by the genes for granulocyte-macrophage colony-stimulating factor and macrophage-colony stimulating factor receptor; all three genes may be implicated in the 5-q syndrome. A translocation between chromosomes 5 and 12, that fuses this gene to that of the translocation, ETV6, leukaemia gene, results in chronic myeloproliferative disorder with eosinophilia.

UOM: 1 * 100 µl

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