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GLMN encodes a phosphorylated protein that is a member of a Skp1-Cullin-F-box-like complex. Additionally we are shipping Glomulin, FKBP Associated Protein Proteins (4) and Glomulin, FKBP Associated Protein Kits (2) and many more products for this protein.
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Human Polyclonal GLMN Primary Antibody for FACS, IHC (p) - ABIN655986
Arai, Kasper, Skaar, Ali, Takahashi, DeCaprio: Targeted disruption of p185/Cul7 gene results in abnormal vascular morphogenesis. in Proceedings of the National Academy of Sciences of the United States of America 2003
Show all 5 references for ABIN655986
Human Polyclonal GLMN Primary Antibody for EIA, FACS - ABIN952528
Brouillard, Vikkula: Vascular malformations: localized defects in vascular morphogenesis. in Clinical genetics 2003
Show all 4 references for ABIN952528
Human Polyclonal GLMN Primary Antibody for IF (p) - ABIN721952
Huang, Xu, Cao, Cao, Zhang: The expression of FOXJ1 in neurogenesis after transient focal cerebral ischemia. in The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2013
Our report contributes to document the possible association between the c.395-1G>C mutation of GLMN gene and glomuvenous malformations.
FAP48 adipocyte expression plays a key role in HIV-associated lipodystrophy.
Structural and biochemical analyses reveal that GLMN adopts a HEAT-like repeat fold that tightly binds the E2-interacting surface of RBX1, inhibiting CRL (show IL31RA Antibodies)-mediated chain formation by the E2 CDC34 (show CDC34 Antibodies).
These data identify glomulin as a permissivity factor for VACV infection and as a potential therapeutic target for inhibition of vaccinia virus (VACV) infection.
The glomuvenous malformation protein Glomulin binds Rbx1 and regulates cullin-1 (show CUL1 Antibodies) RING ligase-mediated turnover of Fbw7 (show FBXW7 Antibodies).
A novel GLMN mutation is described in an Italian family with glomuvenous malformations in which some members present with the less commonly observed phenotype of solitary lesions.
Describes the characterizations of 14 different mutations in the glomulin gene in patients with glomuvenous malformations.
FAP48-FKBP (show FKBP7 Antibodies) complexes increase IL2 (show IL2 Antibodies) production
Results indicate a bacterial adaptation that hijacks inflammasome activation via interactions between IpaH7.8 E3 ubiquitin ligase (show MUL1 Antibodies) and glomulin (GLMN).
The glomulin expression during murine development (E9.5 days post-coitum until adulthood) by non-radioactive in situ hybridization was studied.
This gene encodes a phosphorylated protein that is a member of a Skp1-Cullin-F-box-like complex. The protein is essential for normal development of the vasculature and mutations in this gene have been associated with glomuvenous malformations, also called glomangiomas. Alternatively spliced variants that encode different protein isoforms have been described but the full-length nature of only one has been determined.
glomulin, FKBP associated protein
, FK506-binding protein-associated protein
, FKBP-associated protein
, FKBP associated protein