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human homolog is a diubiquitin protein that may function in antigen processing and presentation [RGD, Feb 2006].. Additionally we are shipping UBD Antibodies (74) and UBD Kits (12) and many more products for this protein.
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Human UBD Protein expressed in Escherichia coli (E. coli) - ABIN667556
Hipp, Kalveram, Raasi, Groettrup, Schmidtke: FAT10, a ubiquitin-independent signal for proteasomal degradation. in Molecular and cellular biology 2005
Show all 2 references for ABIN667556
High expression of FAT10 is associated with glioma.
Study demonstrates how the coordinated interplay of RIG-I (show DDX58 Proteins), TRIM25 (show TRIM25 Proteins), and FAT10 regulate the antiviral innate inflammatory response.
Data suggest that ubiquitin D (UBD) provides a negative feedback on cytokine-induced activation of the endoplasmic reticulum to nucleus signaling 1 (IRE1alpha (show ERN1 Proteins))/c-Jun N-terminal kinase (JNK) pro-apoptotic pathway in cytokine-exposed beta cells.
FAT10 can induce malignant transformation as evidenced from the anchorage-independent growth as well as in vivo tumor-forming abilities of FAT10-overexpressing NeHepLxHT cells.
repertoire of peptides eluted from MHC class I molecules was influenced by FAT10 expression
FAT10 is the only ubiquitin-like modifier known to date which directly targets its hundreds of substrates for degradation by the proteasome. (Review)
Conjugation of the ubiquitin activating enzyme UBE1 (show UBA1 Proteins) with the ubiquitin-like modifier FAT10 targets it for proteasomal degradation
the interaction of FAT10 with MAD2 (show MAD2L1 Proteins) is a key mechanism underlying the promalignant property of FAT10
Results identified a novel HCC (show FAM126A Proteins) regulatory circuit involving FAT10, beta-catenin (show CTNNB1 Proteins)/TCF4 (show TCF4 Proteins), and HOXB9 (show HOXB9 Proteins), the dysfunction of which drives invasive and metastatic character in HCC (show FAM126A Proteins).
STAT3 (show STAT3 Proteins) and NFkappaB (show NFKB1 Proteins) synergistically act for maximum induction of FAT10 expression.
IFNalpha induced FAT10 expression, which is suppressed by ethanol feeding in both HCV(+) and HCV(-) mice
transcription downregulation of the Ufm1 (show UFM1 Proteins) and FAT10 conjugation system in liver Mallory-Denk bodies formation
observations suggest novel roles of FAT10 in immune metabolic regulation that impact aging and chronic disease
FAT10 protects cardiac myocytes against apoptosis.
FAT10 is essential to the induction of Mallory-Denk body formation in di-carbethoxydihydrocollidine fed mice.
FAT10 mediates NF-kappaB (show NFKB1 Proteins) activation and may promote tubulointerstitial inflammation in chronic kidney diseases.
Immunohistochemical studies demonstrated increased FAT10 expression in a model of HIV-associated nephropathy.
These findings indicate that FAT10 may function as a survival factor.
The link between Mallory Denk Body formation and neoplasia formation was likely due to the over expression of UBD (also called FAT10), which is up regulated in 90% of human hepatocellular carcinomas.
human homolog is a diubiquitin protein that may function in antigen processing and presentation
, ubiquitin-like protein FAT10