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Catalogus nummer: (USBIN2915-52N-FITC)

Leverancier: US Biological

Omschrijving: Anti-N-myc Downstream Regulated Gene 1 Protein Rabbit Polyclonal Antibody (FITC (Fluorescein))

UOM: 1 * 200 µl

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Catalogus nummer: (BOSSBS-15444R-CY3)

Leverancier: Bioss

Omschrijving: 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

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Catalogus nummer: (BOSSBS-15444R-FITC)

Leverancier: Bioss

Omschrijving: 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

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Catalogus nummer: (USBIC0115-02L)

Leverancier: US Biological

Omschrijving: Anti-Calcitonin Gene Related Peptide Rabbit Polyclonal Antibody

UOM: 1 * 1 EA

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Catalogus nummer: (BOSSBS-8021R-HRP)

Leverancier: Bioss

Omschrijving: This gene belongs to the chemokine-like factor gene superfamily, a novel family that is similar to the chemokine and the transmembrane 4 superfamilies of signaling molecules. This gene is one of several chemokine-like factor genes located in a cluster on chromosome 16. Alternatively spliced transcript variants containing different 5' UTRs, but encoding the same protein, have been identified. [provided by RefSeq, Jul 2008].

UOM: 1 * 100 µl

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Catalogus nummer: (BOSSBS-6072R-A647)

Leverancier: Bioss

Omschrijving: This gene is a candidate colorectal tumor suppressor gene that is thought to negatively regulate cell cycle progression. The orthologous gene in the mouse expresses a phosphoprotein associated with the plasma membrane and membrane organelles, and overexpression of the mouse protein inhibits entry into S phase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

UOM: 1 * 100 µl

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Catalogus nummer: (USBIN2915-57)

Leverancier: US Biological

Omschrijving: Anti-N-myc Downstream Regulated Gene 1 Protein Rabbit Monoclonal Antibody [clone: 11C1051]

UOM: 1 * 100 µl

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Catalogus nummer: (BOSSBS-15444R-A488)

Leverancier: Bioss

Omschrijving: 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

Sale

Catalogus nummer: (BOSSBS-15444R-A555)

Leverancier: Bioss

Omschrijving: 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

Sale

Catalogus nummer: (BOSSBS-15444R-A680)

Leverancier: Bioss

Omschrijving: 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

Sale

Catalogus nummer: (BOSSBS-3322R-A555)

Leverancier: Bioss

Omschrijving: 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, leukemia gene, results in chronic myeloproliferative disorder with eosinophilia. [provided by RefSeq].

UOM: 1 * 100 µl

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Catalogus nummer: (USBIC0115-01H)

Leverancier: US Biological

Omschrijving: Anti-Calcitonin Gene Related Peptide, alpha Mouse Monoclonal Antibody [clone: 13A93]

UOM: 1 * 100 µl

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Catalogus nummer: (BOSSBS-6165R-A350)

Leverancier: Bioss

Omschrijving: The KRAS gene encodes the human cellular homolog of a transforming gene isolated from the Kirsten rat sarcoma virus. The RAS proteins are GDP/GTP-binding proteins that act as intracellular signal transducers. The most well-studied members of the RAS (derived from 'RAt Sarcoma' virus) gene family include KRAS, HRAS, and NRAS. These genes encode immunologically related proteins with a molecular mass of 21 kD and are homologs of rodent sarcoma virus genes that have transforming abilities. While these wildtype cellular proteins in humans play a vital role in normal tissue signaling, including proliferation, differentiation, and senescence, mutated genes are potent oncogenes that play a role in many human cancers.

UOM: 1 * 100 µl

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Catalogus nummer: (USBIN2566-32D)

Leverancier: US Biological

Omschrijving: Anti-Niemann-Pick Disease, Type C1 Gene-Like 1 Rabbit Polyclonal Antibody

UOM: 1 * 100 µl

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Catalogus nummer: (BOSSBS-9115R-CY5)

Leverancier: Bioss

Omschrijving: Unknown. Candidate gene encoding tumor antigens.Members of the BAGE gene family encode antigens that are recognized by cytotoxic T lymphocytes and are also known as CT (cancer/testis) antigens. Generated by juxtacentromeric shuffling of the MLL3 gene, the ancestral BAGE gene was expanded by acrocentric exchanges and/or juxtacentromeric movements.Generally, BAGE proteins are silent in all normal tissues with the exception of testis. BAGE2 and BAGE 3 (B melanoma antigen 2 and 3, respectively), also known as Cancer/testis antigen 2.2 and 2.3 (respectively), are 109 amino acid secreted proteins that are expressed in 22% of melanomas, lung and bladder carcinomas, and are also expressed in normal testis tissue. Like the genes encoding MAGE proteins, BAGE genes are most likely silenced by DNA methylation and/or chromatin compaction in normal tissues other than testis.

UOM: 1 * 100 µl

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Catalogus nummer: (BOSSBS-8143R-A750)

Leverancier: Bioss

Omschrijving: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC93 (coiled-coil domain containing 93) is a 631 amino acid protein that belongs to the CCDC93 family. CCDC93 is encoded by a gene located on human chromosome 2, which makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene.

UOM: 1 * 100 µl

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