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Anti-SAP30L Antibody

Anti-SAP30L Antibody
Poznámka k dopravě
Dopravné k jednorázové objednávce činí 2.500 Kč, které rozpočítáváme při fakturaci do cen za zboží. V rámci snížení nákladů na dopravu se snažíme konsolidovat objednávky tak, aby se tato suma rozdělila mezi maximum zákazníků. Před objednáním u dodavatele jsou všichni zákazníci vždy předem informovaní o aktuální výši dopravy.
Anti-SAP30L Antibody
SAP30L rabbit polyclonal primary antibody from PhosphoSolutions is produced in-house. It detects hu...
12 139,00Kč
Cena bez DPH: 10 032,23Kč

Dostupné možnosti

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Dotaz na zboží

Ondřej Hovorka Ph.D.

Výkonný ředitel

SAP30L rabbit polyclonal primary antibody from PhosphoSolutions is produced in-house. It detects human SAP30L and is antigen affinity purified. It is great for use in WB. A novel TGF- beta up-regulated mRNA species, the Sin3-associated protein 30-like, SAP30L has been identified. The predicted nuclear localization signal of SAP30L is sufficient for nuclear transport of the protein although mutating it does not completely remove SAP30L from the nuclei. By reason of its nuclear localization and close homology to SAP30 it is thought that SAP30L might have a role in recruiting the Sin3-histone deacetylase complex to specific co-repressor complexes in response to TGF-beta, leading to the silencing of proliferation-driving genes in the differentiating intestinal epithelial cells.
Technické specifikace
Doprava a skladování Blue Ice
Vlastnosti
Aplikace WB
Izotyp IgG
Klon polyclonal
Původ Rabbit
Specifita Reacts with the C-terminal region of human SAP30L. Detects wild-type transfected hSAP30L or GST-hSAP30L fusion protein as well as endogenous hSAP30L in human cell lines (e.g., HEK293 and MCF-7 cells). Detects wild-type transfected hSAP30L or GST-hSAP30L fusion protein in non-human cell lines (e.g., NIH3T3 cells), but does not detect endogenous non-human SAP30L. The transfected wild-type hSAP30L runs with an apparent molecular weight of ~30kDa and the endogenous hSAP30L band runs with an apparent molecular weight of 21-22 kDa. The difference in the size of the bands is unknown, but is seen by investigators in all studies of hSAP30L. Possible explanations for the size difference may be to cleavage product, degradation and/or product or post-translational modification.
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