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Descripción: DOM3Z, also known as NG6 or DOM3L, is a 396 amino acid ubiquitously expressed protein belonging to the Dom3Z family. The gene encoding DOM3Z maps to human chromosome 6 in the major histocompatibility complex (MHC) class III region. Chromosome 6 contains 170 million base pairs and comprises nearly 6% of the human genome. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. Additionally, Porphyria cutanea tarda, Parkinson's disease and Stickler syndrome are all associated with genes that map to chromosome 6.
Numero del catalogo: BOSSBS-9054R-CY5
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Component of the post-replicative DNA mismatch repair system (MMR). Heterodimerizes with MSH2 to form MutS beta which binds to DNA mismatches thereby initiating DNA repair. When bound, the MutS beta heterodimer bends the DNA helix and shields approximately 20 base pairs. MutS beta recognizes large insertion-deletion loops (IDL) up to 13 nucleotides long. After mismatch binding, forms a ternary complex with the MutL alpha heterodimer, which is thought to be responsible for directing the downstream MMR events, including strand discrimination, excision, and resynthesis.
Numero del catalogo: BOSSBS-8542R-A555
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Component of the post-replicative DNA mismatch repair system (MMR). Heterodimerizes with MSH2 to form MutS beta which binds to DNA mismatches thereby initiating DNA repair. When bound, the MutS beta heterodimer bends the DNA helix and shields approximately 20 base pairs. MutS beta recognizes large insertion-deletion loops (IDL) up to 13 nucleotides long. After mismatch binding, forms a ternary complex with the MutL alpha heterodimer, which is thought to be responsible for directing the downstream MMR events, including strand discrimination, excision, and resynthesis.
Numero del catalogo: BOSSBS-8542R-A488
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Component of the post-replicative DNA mismatch repair system (MMR). Heterodimerizes with MSH2 to form MutS beta which binds to DNA mismatches thereby initiating DNA repair. When bound, the MutS beta heterodimer bends the DNA helix and shields approximately 20 base pairs. MutS beta recognizes large insertion-deletion loops (IDL) up to 13 nucleotides long. After mismatch binding, forms a ternary complex with the MutL alpha heterodimer, which is thought to be responsible for directing the downstream MMR events, including strand discrimination, excision, and resynthesis.
Numero del catalogo: BOSSBS-8542R-A647
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human KCNE1.
Numero del catalogo: ABNOH00003753-AP11
UOM: 1 * 1 SET
Proveedor: Abnova


Descripción: Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a member of the histone H4 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. [provided by RefSeq, Jul 2008].
Numero del catalogo: BOSSBS-4706R-CY7
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Nrarp (NOTCH-regulated ankyrin repeat protein) is a 114 amino acid protein that contains two ANK repeats and is thought to play a role in the formation of somites. The gene encoding Nrarp maps to human chromosome 9, which contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia 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.
Numero del catalogo: BOSSBS-11914R-CY7
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a member of the histone H4 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. [provided by RefSeq, Jul 2008].
Numero del catalogo: BOSSBS-4706R
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Sodio dodecilsulfato (SDS) ≥97.0% (by titrimetric analysis) para cromatografía en par iónico
Numero del catalogo: TCIAI0352-500G
UOM: 1 * 500 g
Proveedor: TCI


Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human T.
Numero del catalogo: ABNOH00006862-AP61
UOM: 1 * 1 SET
Proveedor: Abnova


Descripción: The protein encoded by this gene is a smooth muscle myosin belonging to the myosin heavy chain family. The gene product is a subunit of a hexameric protein that consists of two heavy chain subunits and two pairs of non-identical light chain subunits. It functions as a major contractile protein, converting chemical energy into mechanical energy through the hydrolysis of ATP. The gene encoding a human ortholog of rat NUDE1 is transcribed from the reverse strand of this gene, and its 3' end overlaps with that of the latter. The pericentric inversion of chromosome 16[inv(16)(p13q22)] produces a chimeric transcript that encodes a protein consisting of the first 165 residues from the N terminus of core-binding factor beta in a fusion with the C-terminal portion of the smooth muscle myosin heavy chain. This chromosomal rearrangement is associated with acute myeloid leukemia of the M4Eo subtype. Alternative splicing generates isoforms that are differentially expressed, with ratios changing during muscle cell maturation. Alternatively spliced transcript variants encoding different isoforms have been identified. MYH11 is a smooth muscle myosin belonging to the myosin heavy chain family. It is a subunit of a hexameric protein that consists of two heavy chain subunits and two pairs of non-identical light chain subunits. It functions as a major contractile protein, converting chemical energy into mechanical energy through the hydrolysis of ATP.
Numero del catalogo: BOSSBS-1956R-A555
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: Este guante tejido de Spandex/nylon tiene un revestimiento ¾ sumergido de neopreno/nitrilo que proporciona repelencia al aceite. Ideal para su uso en ambientes aceitosos.
Numero del catalogo: 112-4291
UOM: 1 * 12 Par
Proveedor: Ansell


Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human SGOL1.
Numero del catalogo: ABNOH00151648-AP51
UOM: 1 * 1 SET
Proveedor: Abnova


Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human PLSCR3.
Numero del catalogo: ABNOH00057048-AP51
UOM: 1 * 1 SET
Proveedor: Abnova


Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human CD58.
Numero del catalogo: ABNOH00000965-AP51
UOM: 1 * 1 SET
Proveedor: Abnova


Descripción: This Set comes with matched Antibody Pair to detect and quantify protein level of human FAS.
Numero del catalogo: ABNOH00000355-AP51
UOM: 1 * 1 SET
Proveedor: Abnova


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