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anti-Human C1QBP Antikörper:
anti-Mouse (Murine) C1QBP Antikörper:
anti-Rat (Rattus) C1QBP Antikörper:
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Hepatitis C virus core protein ligates gC1qR to induce A20 (zeige TNFAIP3 Antikörper) expression in macrophages via P38 (zeige CRK Antikörper), JNK (zeige MAPK8 Antikörper) and NF-kappaB (zeige NFKB1 Antikörper) signaling pathways, which leads to a low-grade chronic inflammation during HCV infection.
The RAP80 (zeige UIMC1 Antikörper) deficiency reduces the protein level of p32 and p32 dependent mitochondrial translating proteins such as Rieske and COX1 (zeige COX1 Antikörper).
Mutation in C1QBP gene is associated with Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies.
results implicate p32 as a key host factor for RSV virus production, and bring to light the potential importance of mitochondria in RSV infection
single nucleotide polymorphism srs2285747 of HABP1 increased breast cancer risk and elevated its protein expression in northern Chinese women
The authors identified Importin-alpha1 to bind to Coxiella burnetii AnkG and concluded that binding of AnkG to p32 and Importin-alpha1 is essential for its migration into the nucleus.
HABP1 overexpression is associated with cervical cancer.
This study supports a key role for gC1qR in malaria-associated endovascular pathogenesis
these data suggest that C1QBP could regulate YBX1 (zeige YBX1 Antikörper) to suppress the AR-enhanced RCC (zeige XRCC1 Antikörper) cell invasion. Targeting this newly identified C1QBP/YBX1 (zeige YBX1 Antikörper)/AR/MMP9 (zeige MMP9 Antikörper) signal pathway may provide a new potential therapy to better suppress RCC (zeige XRCC1 Antikörper) metastasis.
C1QBP interacts with DLAT (zeige DLAT Antikörper) and regulates the enzyme activity of pyruvate dehydrogenase (zeige PDP Antikörper).
macrophage/neutrophil-specific p32 conditional knockout mice showed exacerbated inflammation and reduced survival in response to LPS. Based on these findings, p32 is an important regulator of inflammatory signaling and is a potential drug candidate for treatment of sepsis in mammals.
application of p33 (zeige LTB Antikörper) significantly improved survival in mice receiving an otherwise lethal dose of histones.
Authors propose that p32 is required for functional mitoribosome formation to synthesize proteins within mitochondria.
we have identified a mitochondrial protein (zeige COX6B2 Antikörper) p32 as a novel interactor of parkin (zeige PARK2 Antikörper) in the brain
C1qbp could directly bind to CypD. Therefore C1qbp appears to act as an endogenous inhibitor of the MPT pore, most likely through binding to CypD, and thus protects cells against oxidative stress.
Intracellular localization and further functional studies suggested that CHCHD2 and HABP1 may mutually regulate each other to balance cell migration.
Rat and mouse homologs of the HABP1 pseudogene also contain multiple mutations, leading to the insertion of premature stop codons confirming the identity of a processed pseudogene.
Study demonstrates the differential expression of HABP1 during progression of epidermal carcinoma.
p32 phosphorylation by ATM (zeige ATM Antikörper) might be a new transcriptional regulatory pathway for specific DNA damage responses in heart.
The human complement subcomponent C1q associates with C1r and C1s in order to yield the first component of the serum complement system. The protein encoded by this gene is known to bind to the globular heads of C1q molecules and inhibit C1 activation. This protein has also been identified as the p32 subunit of pre-mRNA splicing factor SF2, as well as a hyaluronic acid-binding protein.
p32 subunit of splicing factor SF2
, 38k protein
, complement component 1, q subcomponent binding protein
, ASF/SF2-associated protein p32
, C1q globular domain-binding protein
, complement component 1 Q subcomponent-binding protein, mitochondrial
, glycoprotein gC1qBP
, hyaluronan-binding protein 1
, mitochondrial matrix protein p32
, splicing factor SF2-associated protein
, GC1q-R protein