Hai cercato: genomes

Codice catalogo: (BOSSBS-9669R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-9669R-CY7

Codice articolo locale: BOSSBS-9669R-CY7

Descrizione: DENND4C is a 1,673 amino acid multi-pass membrane protein. DENND4C contains a dDENN domain, DENN domain, uDENN domain and a PPR (pentatricopeptide) repeat. As a result of alternative splicing, six DENND4C isoforms exist. The gene encoding DENND4C maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-11629R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-11629R-HRP

Codice articolo locale: BOSSBS-11629R-HRP

Descrizione: Olfactory receptors are G protein-coupled receptors that localize to the cilia of olfactory sensory neurons where they display affinity for and bind to a variety of odor molecules. The genes encoding olfactory receptors comprise the largest family in the human genome. The binding of olfactory receptor proteins to odor molecules triggers a signal transduction that propagates nerve impulses throughout the body, ultimately leading to transmission of the signal to the brain and the subsequent perception of smell. OR10J3 (olfactory receptor 10J3) is a 329 amino acid protein. The gene encoding OR10J3 maps to human chromosome 1.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-6405R)

Fornitore: Bioss

Codice articolo fornitore: BS-6405R

Codice articolo locale: BOSSBS-6405R

Descrizione: Get4 is a 327 amino acid cytoplasmic protein that exists as two alternatively spliced isoforms. Get4 forms a multiprotein complex, known as the BAT3 complex, with UBL4A, BAT3 and ARSA. The BAT3 complex plays a role in transporting tail-anchored membrane proteins to the endoplasmic reticulum membrane. The gene encoding Get4 maps to human chromosome 7p22.3. Human chromosome 7 houses over 1,000 genes, comprises nearly 5% of the human genome and has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.

UOM: 1 * 100 µl

Promo

Codice catalogo: (PRSI7435)

Fornitore: ProSci Inc.

Codice articolo fornitore: 7435

Codice articolo locale: PRSI7435

Descrizione: Heartland Virus Glycoprotein 2 Antibody: The Heartland virus is a newly identified member of the phlebovirus genus of the Bunyaviridae family. Initial reports indicate that symptoms may include fever, fatigue, diarrhea, thrombocytopenia, and leukopenia. The Bunyaviridae family of viruses are spherical enveloped viruses with a tripartite RNA genome of negative or ambisense polarity. The glycoprotein RNA encodes a polyprotein that is cleaved into the G1 and G2 proteins.

UOM: 1 * 100 µG

Promo

Codice catalogo: (BOSSBS-11075R)

Fornitore: Bioss

Codice articolo fornitore: BS-11075R

Codice articolo locale: BOSSBS-11075R

Descrizione: CNTNAP3B is a 1,288 amino acid protein that is encoded by a gene which maps to human chromosome 9. Chromosome 9 contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in translocations that lead to the aberrant production of a BCR-ABL fusion protein often found in leukemias.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-2168R-CY5.5)

Fornitore: Bioss

Codice articolo fornitore: BS-2168R-CY5.5

Codice articolo locale: BOSSBS-2168R-CY5.5

Descrizione: ADAR1 converts adenosine to inosine in dsRNA, which destabilizes the dsRNA helix. This activity is important for various functions like site-specific RNA editing of transcripts of the glutamate receptors and modifying viral RNA genomes (which may be responsible for hypermutation of certain negative-stranded viruses, e.g., measles virus). ADAR1 also binds to short interfering RNAs (siRNA) without editing them and suppresses siRNA-mediated RNA interference. This protein is ubiquitously expressed, with the highest levels being found in brain and lung.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-1557G-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-1557G-FITC

Codice articolo locale: BOSSBS-1557G-FITC

Descrizione: Hepatitis B Virus (HBV) infection induces a disease state characterised by liver damage, inflammation and viral persistence. Infection also increases the risk of hepatocellular carcinoma. HBV belongs to the Hepadnaviridae family of viruses. Its genome consists of partially double stranded circular DNA. The DNA is enclosed in a nucleocapsid, or core antigen (HBcAg), which is surrounded by a spherical envelope (surface antigen or HBsAg). The core antigen shares its sequences with the e antigen (HBeAg) but no cross reactivity between the two proteins has been observed. The HBV genome also encodes a DNA polymerase that also acts as a reverse transcriptase. Hepatitis B infection is normally diagnosed from serological tests that detect HBsAg but as the disease progresses this antigen may no longer be present in the blood and tests for HBcAg are used. If HBsAg can be detected in the blood for longer than six months, chronic hepatitis B is diagnosed. The antigenic determinant of the protein moiety of the HBsAg determines specific characteristics of different serotypes and provides the basis of immunodetection. HBsAg has antigenic heterogeneity, specifically, two pairs of sub specific determinants, d/y and w/r allow the following combinations: adw, ayw, adr, ayr.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13323R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-13323R-HRP

Codice articolo locale: BOSSBS-13323R-HRP

Descrizione: GCSH is a 173 amino acid mitochondrial protein that contains one lipoyl-binding domain and belongs to the gcvH family. Defects in the gene encoding GCSH are the cause of glycine encephalopathy (GCE), an autosomal recessive disease that is also referred to as non-ketotic hyperglycinemia (NKH). Characterized by severe neurological symptoms, patients with GCE have a large amount of glycine accumulated in their body fluids. The gene encoding GCSH maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-2168R-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-2168R-FITC

Codice articolo locale: BOSSBS-2168R-FITC

Descrizione: ADAR1 converts adenosine to inosine in dsRNA, which destabilizes the dsRNA helix. This activity is important for various functions like site-specific RNA editing of transcripts of the glutamate receptors and modifying viral RNA genomes (which may be responsible for hypermutation of certain negative-stranded viruses, e.g., measles virus). ADAR1 also binds to short interfering RNAs (siRNA) without editing them and suppresses siRNA-mediated RNA interference. This protein is ubiquitously expressed, with the highest levels being found in brain and lung.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13323R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-13323R-A680

Codice articolo locale: BOSSBS-13323R-A680

Descrizione: GCSH is a 173 amino acid mitochondrial protein that contains one lipoyl-binding domain and belongs to the gcvH family. Defects in the gene encoding GCSH are the cause of glycine encephalopathy (GCE), an autosomal recessive disease that is also referred to as non-ketotic hyperglycinemia (NKH). Characterized by severe neurological symptoms, patients with GCE have a large amount of glycine accumulated in their body fluids. The gene encoding GCSH maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-4982R)

Fornitore: Bioss

Codice articolo fornitore: BS-4982R

Codice articolo locale: BOSSBS-4982R

Descrizione: HIV1 performs highly complex orchestrated tasks during the assembly, budding, maturation and infection stages of the viral replication cycle. During viral assembly, the proteins form membrane associations and self-associations that ultimately result in budding of an immature virion from the infected cell. Gag precursors also function during viral assembly to selectively bind and package two plus strands of genomic RNA. HIV1 Gag p17, the HIV1 matrix protein is produced by the digestion of its precursor Gag p55 by HIV1 protease.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-4982R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-4982R-A680

Codice articolo locale: BOSSBS-4982R-A680

Descrizione: HIV1 performs highly complex orchestrated tasks during the assembly, budding, maturation and infection stages of the viral replication cycle. During viral assembly, the proteins form membrane associations and self-associations that ultimately result in budding of an immature virion from the infected cell. Gag precursors also function during viral assembly to selectively bind and package two plus strands of genomic RNA. HIV1 Gag p17, the HIV1 matrix protein is produced by the digestion of its precursor Gag p55 by HIV1 protease.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13323R)

Fornitore: Bioss

Codice articolo fornitore: BS-13323R

Codice articolo locale: BOSSBS-13323R

Descrizione: GCSH is a 173 amino acid mitochondrial protein that contains one lipoyl-binding domain and belongs to the gcvH family. Defects in the gene encoding GCSH are the cause of glycine encephalopathy (GCE), an autosomal recessive disease that is also referred to as non-ketotic hyperglycinemia (NKH). Characterized by severe neurological symptoms, patients with GCE have a large amount of glycine accumulated in their body fluids. The gene encoding GCSH maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome.

UOM: 1 * 100 µl

Promo

Codice catalogo: (PRSI7433)

Fornitore: ProSci Inc.

Codice articolo fornitore: 7433

Codice articolo locale: PRSI7433

Descrizione: Heartland Virus Glycoprotein 1 Antibody: The Heartland virus is a newly identified member of the phlebovirus genus of the Bunyaviridae family. Initial reports indicate that symptoms may include fever, fatigue, diarrhea, thrombocytopenia, and leukopenia. The Bunyaviridae family of viruses are spherical enveloped viruses with a tripartite RNA genome of negative or ambisense polarity. The glycoprotein RNA encodes a polyprotein that is cleaved into the G1 and G2 proteins.

UOM: 1 * 100 µG

Promo

Codice catalogo: (BOSSBS-9669R)

Fornitore: Bioss

Codice articolo fornitore: BS-9669R

Codice articolo locale: BOSSBS-9669R

Descrizione: DENND4C is a 1,673 amino acid multi-pass membrane protein. DENND4C contains a dDENN domain, DENN domain, uDENN domain and a PPR (pentatricopeptide) repeat. As a result of alternative splicing, six DENND4C isoforms exist. The gene encoding DENND4C maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-6405R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-6405R-A680

Codice articolo locale: BOSSBS-6405R-A680

Descrizione: Get4 is a 327 amino acid cytoplasmic protein that exists as two alternatively spliced isoforms. Get4 forms a multiprotein complex, known as the BAT3 complex, with UBL4A, BAT3 and ARSA. The BAT3 complex plays a role in transporting tail-anchored membrane proteins to the endoplasmic reticulum membrane. The gene encoding Get4 maps to human chromosome 7p22.3. Human chromosome 7 houses over 1,000 genes, comprises nearly 5% of the human genome and has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.

UOM: 1 * 100 µl

Promo