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The protein encoded by PRAM1 is similar to FYN binding protein (FYB/SLAP-130), an adaptor protein involved in T cell receptor mediated signaling. Additionally we are shipping PML-RARA Regulated Adaptor Molecule 1 Antibodies (36) and PML-RARA Regulated Adaptor Molecule 1 Kits (2) and many more products for this protein.
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A yopH mutant survived better in the absence of neutrophils, indicating that neutrophil inactivation by YopH by targeting PRAM-1/SKAP-HOM (show SKAP2 Proteins) and SLP-76 (show LCP2 Proteins)/Vav (show VAV1 Proteins)/PLCgamma2 (show PLCG2 Proteins) signaling hubs may be critical for Yersinia survival.
autophagy contributes to the anti-apoptotic function of the PML (show PML Proteins)-RARalpha (show RARA Proteins) protein through inhibiting the Akt (show AKT1 Proteins)/mTOR (show FRAP1 Proteins) pathway
Transgenic mice expressing PML-RAR alpha (show RARA Proteins) develop acute promyelocytic leukemia (show PML Proteins) with long latency, low penetrance, and acquired cytogenetic abnormalities.
Our results show that the pretreatment PML (show PML Proteins)-RARA (show RARA Proteins) molecular burden could therefore be used to improve risk stratification in order to develop more individualized treatment regimens for high-risk APL (show FASL Proteins) cases.
The 3-plex RT-qPCR assay is a specific, sensitive, stable, and cost-effective method that can be used for the rapid diagnosis and treatment monitoring of acute promyelocytic leukemia (show PML Proteins) with PML (show PML Proteins)-RARa (show RARA Proteins)
The MIR125B1-mediated blockade of PML (show PML Proteins)-RARA (show RARA Proteins) proteolysis was regulated via an autophagy-lysosomal pathway, contributing to the inhibition of acute promyelocytic leukemia (show PML Proteins) differentiation.
PRAM-1 is required for optimal integrin-dependent neutrophil function.
Caspase 3 (show CASP3 Proteins)-cleaved SH3 domain of HIP-55 (show DBNL Proteins) is likely involved in PRAM-1-mediated JNK (show MAPK8 Proteins) activation upon arsenic trioxide-induced differentiation of NB4 cells.
The use of reverse-transcription polymerase chain reaction for the detection of the PML (show PML Proteins)-RARA (show RARA Proteins) and RARA (show RARA Proteins)-PML (show PML Proteins) fusion genes that allow for monitoring of acute myelocytic leukemia.
PML (show PML Proteins)-RARalpha (show RARA Proteins) fusion transcripts have been shown to be useful markers for establishing the diagnosis and for monitoring the response to treatment of acute promyelocytic leukemia (show PML Proteins).
Interaction of PRAM-1 and hSH3 domains of adhesion and degranulation promoting adapter protein (show TOLLIP Proteins) (ADAP (show FYB Proteins)) with phosphatidylcholine (show SGMS2 Proteins)-containing liposomes is observed upon incorporation of phosphatidylserine or phosphoinositides into the membrane bilayer.
hidden abnormalities and novel disease-related genomic changes occur in t(15;17)translocation in acute promyelocytic leukemia (show PML Proteins) formation of PML (show PML Proteins)-RARA (show RARA Proteins) gene
The protein encoded by this gene is similar to FYN binding protein (FYB/SLAP-130), an adaptor protein involved in T cell receptor mediated signaling. This gene is expressed and regulated during normal myelopoiesis. The expression of this gene is induced by retinoic acid and is inhibited by the expression of PML-RARalpha, a fusion protein of promyelocytic leukemia (PML) and the retinoic acid receptor-alpha (RARalpha).
PML-RARA regulated adaptor molecule 1
, PML-RARA-regulated adapter molecule 1-like
, PML-RARA-regulated adapter molecule 1
, PML-RARA target gene encoding an Adaptor Molecule-1
, PML-RAR alpha-regulated adaptor molecule 1