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The protein encoded by MYCBP binds to the N-terminus of the oncogenic protein C-MYC, enhancing the ability of C-MYC to activate E box-dependent transcription. De plus, nous expédions C-Myc Binding Protein Kits (28) et C-Myc Binding Protein Protéines (12) et beaucoup plus de produits pour cette protéine.
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Cow (Bovine) Polyclonal MYCBP Primary Antibody pour IHC, WB - ABIN2777462
Furusawa, Taira, Iguchi-Ariga, Ariga: AMY-1 interacts with S-AKAP84 and AKAP95 in the cytoplasm and the nucleus, respectively, and inhibits cAMP-dependent protein kinase activity by preventing binding of its catalytic subunit to A-kinase-anchoring protein (AKAP) complex. dans The Journal of biological chemistry 2002
Show all 3 Pubmed References
c-Myc expression is reduced in pterygium compared with normal conjunctiva.
Suppression of telomerase activity mediated by PinX1 is involved in the Mad1/c-Myc pathway.
miR-22 acts as a tumor suppressor through direct repression of MYCBP expression and subsequent reduction of oncogenic c-Myc activities.
identified a novel AMY-1-binding protein, AAT-1, and determied its expression profiles, genes, and cellular localization; results showed that AAT-1 was specifically expressed in the testis throughout spermatogenesis and was also present in mature sperm
interacts with S-AKAP84 and AKAP95 in the cytoplasm and the nucleus, respectively, and inhibits enzyme acdtivity by preventing binding of its catalytic subunit to A-kinase-anchoring protein (AKAP) complex
AMY-1 coordinates ADP-Ribosylation Factors-mediated membrane trafficking and signaling pathways.
An important role for MBP-1 in the altered cell proliferation and energy utilization that occur in response to an altered glucose concentration.
AMY-1 was localized in the mitochondria of HeLa and sperm in association with AKAP149 and S-AKAP84, respectively. These results suggest that AMY-1 plays a role in spermatogenesis
L-Myc, as well as c-Myc mutants (W136E and dN2), all of which have little transformation activity, promoted human iPSC generation more efficiently and specifically compared with WT c-Myc.
These data suggested that hAECs can alter mouse ESC gene expression via epigenetic modification of c-Myc, providing a possible mechanism for the hAEC-induced maintenance of ESCs in an undifferentiated state.
The advantage of this system over the traditional retroviral infection is the ability to turn the genes on and off so that the kinetics of reprogramming and gene expression requirements can be analyzed in detail.
The protein encoded by this gene binds to the N-terminus of the oncogenic protein C-MYC, enhancing the ability of C-MYC to activate E box-dependent transcription. The encoded protein is normally found in the cytoplasm, but it translocates to the nucleus during S phase of the cell cycle and associates with C-MYC. This protein may be involved in spermatogenesis. This gene can be silenced by microRNA-22. Two transcript variants, one protein-coding and the other probably not protein-coding, have been found for this gene.
, associate of myc-1
, c-myc binding protein
, associate of Myc 1
, LOW QUALITY PROTEIN: C-Myc-binding protein