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Antilichamen Elabscience biedt een breed scala aan gegarandeerde en goed geselecteerde monoklonale en polyklonale antilichamen, fosfo-antilichamen, acetyl-antilichamen, tag-antilichamen, secundaire antilichamen, isotype-antilichamen, enz. Als professionele leverancier van antilichamen, zijn Elabscience-antilichaamproducten strikt gevalideerd om de zuiverheid te garanderen en kwaliteit. Onze primaire antilichamen en secundaire antilichamen die specifiek zijn voor een verscheidenheid aan soorten en breed kunnen worden toegepast in ELISA, WB, IHC en IF. Welkom bij het aanvragen van diensten voor de productie van antilichamen of koop online antilichamen bij Elabscience®. Bekijk alle antilichaamproducten
Verschillende gevalideerde flowcytometrie-antilichamen van Elabscience bieden meerdere kleurstofkeuzes en een breed scala aan zowel intracellulaire als extracellulaire doelen. Vind hier uw doel-FCM-antilichamen. Elabscience Flowcytometrie Antilichamen
Alle antilichamen van Elabscience voor kankeronderzoek zijn volledig gevalideerd door ons R&D-team, met uitgebreide en nauwkeurige experimentele gegevens. Klik om meer details over Elabscience-antilichamen voor kankeronderzoek te bekijken.
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19.
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined.
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced.
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Description: This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.
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