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The protein encoded by NAP1L4 is a platelet-derived growth factor that belongs to the CXC chemokine family. De plus, nous expédions NAP1L4 Anticorps (37) et NAP1L4 Protéines (9) et beaucoup plus de produits pour cette protéine.
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knockdown of NAP1L1 (Montrer NAP1L1 Kits ELISA) suppresses IkappaBalpha (Montrer NFKBIA Kits ELISA) degradation and nuclear transport of p65 subunit after treatment with TNF-a stimulation, leading to attenuation of the NF-kappaB (Montrer NFKB1 Kits ELISA) transcriptional activity, whereas NAP1L4 knockdown remains silent.results of this study suggest that NAP1L1 (Montrer NAP1L1 Kits ELISA) downregulation renders the cell vulnerable to apoptotic cell death through attenuation of NF-kappaB (Montrer NFKB1 Kits ELISA) transcriptional activity on the anti-apop...
Results identified several proteins interacting with NAP1L2, including the ubiquitously expressed members of the nucleosome assembly protein family, NAP1L1 (Montrer NAP1L1 Kits ELISA) and NAP1L4.
Telomeric NAP1L4 and OSBPL5 of the KCNQ1 (Montrer KCNQ1 Kits ELISA) cluster, and the DECORIN (Montrer DCN Kits ELISA) gene are not imprinted in human trophoblast stem cells.
The biochemical properties of two human NAP1 (Montrer IL8 Kits ELISA)-like proteins, hNAP1L1 and hNAP1L4, were characterized.
NAP-2 is in complex(es) with other proteins, which are distinct from histones
Human Nap2 promotes nucleosome assembly with H3t (Montrer HIST3H3 Kits ELISA)/H4.
imprinting status of four cattle genes (Tssc4,Nap1l4, Phlda2 and Osbpl5) in seven types of tissues, were assessed in cattle.
Leukocyte migration is initiated by homotypic adhesive interactions between platelets, leading to the development of an NAP-2 (Montrer PPBP Kits ELISA) chemotactic gradient within the thrombus body that guides leukocytes to sites of vascular injury.
This gene encodes a member of the nucleosome assembly protein (NAP) family which can interact with both core and linker histones. It can shuttle between the cytoplasm and nucleus, suggesting a role as a histone chaperone. This gene is one of several located near the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer.
, nucleosome assembly protein 1-like 4b
, nucleosome assembly protein 2
, nucleosome assembly protein 1-like 4
, no arches-like zinc finger protein
, nucleosome assembly protein 1 like 4