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anti-Human TRIM32 Antibodies:
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Human Monoclonal TRIM32 Primary Antibody for IF, RNAi - ABIN524889
Schwamborn, Berezikov, Knoblich: The TRIM-NHL protein TRIM32 activates microRNAs and prevents self-renewal in mouse neural progenitors. in Cell 2009
Show all 5 Pubmed References
Cow (Bovine) Polyclonal TRIM32 Primary Antibody for WB - ABIN2780865
Chiang, Beck, Yen, Tayeh, Scheetz, Swiderski, Nishimura, Braun, Kim, Huang, Elbedour, Carmi, Slusarski, Casavant, Stone, Sheffield: Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11). in Proceedings of the National Academy of Sciences of the United States of America 2006
Show all 3 Pubmed References
Human Polyclonal TRIM32 Primary Antibody for ICC, IF - ABIN443593
Fatima, Kumari, Schwamborn, Mahadevan, Shankar, Raja, Seth: Tripartite containing motif 32 modulates proliferation of human neural precursor cells in HIV-1 neurodegeneration. in Cell death and differentiation 2016
Show all 2 Pubmed References
Human Polyclonal TRIM32 Primary Antibody for ELISA, WB - ABIN564975
Sato, Okumura, Iguchi, Ariga, Hatakeyama: TRIM32 promotes retinoic acid receptor ?-mediated differentiation in human promyelogenous leukemic cell line HL60. in Biochemical and biophysical research communications 2012
TRIM32 as a crucial positive regulator of Herpes Simplex Virus type 1 (HSV-1) induced IFN-beta (show IFNB1 Antibodies) production in corneal epithelial cells, and it played a predominant role in clearing HSV-1 from the cornea.
HSP70 (show HSP70 Antibodies)-TRIM32 complex is biochemically distinct from the previously characterized 14-3-3 (show YWHAQ Antibodies)-TRIM32 phospho-complex.
Data suggest that, in cardiomyocytes, TRIM32 attenuates activation of SRF signaling and hypertrophy due to dysbindin; TRIM24 promotes these effects. TRIM32 promotes dysbindin degradation; TRIM24 protects dysbindin from degradation. (TRIM = tripartite motif-containing protein; SRF = serum response factor)
Duchenne muscular dystrophy (show DMD Antibodies) muscles showed a selective up-regulation of the ubiquitin ligase tripartite motif-containing protein 32 (TRIM32). The induction of TRIM32 was due to a transcriptional effect and it correlated with disease severity.
we provide a detailed characterization of the TRIM (show TRAT1 Antibodies) ligases TRIM25 (show TRIM25 Antibodies) and TRIM32 and show how their oligomeric state is linked to catalytic activity
that TRIM32 plays a protective role in aortic banding-induced pathological cardiac remodelling by blocking Akt (show AKT1 Antibodies)-dependent signalling
these findings suggest that TRIM32 might play important roles in the hepatocarcinogenesis.
results show a novel molecular cascade involving miR (show MLXIP Antibodies)-155 and TRIM32 leading to HIV-1 Tat (show TAT Antibodies)-induced attenuated proliferation of neural precursor cells; study also uncovered an unidentified role for miR (show MLXIP Antibodies)-155 in modulating human neural stem cell proliferation, helping in better understanding of neural precursor cells and diseased brain
Studies indicate most-studied TRIpartite Motif (TRIM (show TRAT1 Antibodies))-NHL (show RTEL1 Antibodies) proteins TRIM2 (show TRIM2 Antibodies), TRIM3 (show TRIM3 Antibodies), TRIM32 and TRIM71 (show TRIM71 Antibodies), and their mutations have been linked to diseases.
Results suggest that Salmonella effector SseK3 binding to host tripartite motif-containing 32 protein (TRIM32) in the inhibition of nuclear factor kappa B (NF-kappaB (show NFKB1 Antibodies)) activation: [SseK3]
TRIM32 protein expression is defective in atopic dermatitis lesional skin.
In summary, the data presented here reveal that TRIM32 directly regulates at least two of the four Yamanaka Factors (cMyc (show MYC Antibodies) and Oct4 (show POU5F1 Antibodies)), to modulate cell fate transitions.
TRIM32 represents a model of intrinsic immunity, in which a host protein directly senses and counters viral infection in a species specific fashion by directly limiting viral replication
NDRG2 (show NDRG2 Antibodies) accumulated in skeletal muscle and myoblasts in the absence of TRIM32. NDRG2 (show NDRG2 Antibodies) overexpression in myoblasts led to reduced cell proliferation and delayed cell cycle withdrawal during differentiation.
TRIM32 overexpression promotes cell oncogenic transformation and tumorigenesis in mice in a largely p53 (show TP53 Antibodies)-dependent manner.
Data show that RNA helicase DDX6 (show DDX6 Antibodies) colocalizes with ubiquitin-protein ligase (show UBE2K Antibodies) TRIM32 in neural stem cells and neurons and that it increases the activity of microRNA Let-7a.
TRIM32 plays important roles in regulation of hyperactivities and positively regulates the development of anxiety and depression disorders induced by chronic stress.
The results highlight the function of the cell fate-determinant TRIM32 for a balanced activity of the adult neurogenesis process.
The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. The protein has also been localized to the nucleus, where it interacts with the activation domain of the HIV-1 Tat protein. The Tat protein activates transcription of HIV-1 genes.
E3 ubiquitin-protein ligase TRIM32
, tripartite motif-containing 32
, TAT-interactive protein, 72-KD
, tripartite motif containing 32
, 72 kDa Tat-interacting protein
, tripartite motif-containing protein 32
, zinc finger protein HT2A
, zinc-finger protein HT2A
, bM468K2.2 (tripartite motif protein 32)
, tripartite motif protein 32
, zinc finger protein 117