Recombinant Human ANAPC11 293 Cell Lysate
Cat.No. : | ANAPC11-8870HCL |
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Description : | Antigen standard for anaphase promoting complex subunit 11 (ANAPC11), transcript variant 5 is a lysate prepared from HEK293T cells transiently transfected with a TrueORF gene-carrying pCMV plasmid and then lysed in RIPA Buffer. Protein concentration was determined using a colorimetric assay. The antigen control carries a C-terminal Myc/DDK tag for detection. |
Source : | HEK 293 cells |
Species : | Human |
Components : | This product includes 3 vials: 1 vial of gene-specific cell lysate, 1 vial of control vector cell lysate, and 1 vial of loading buffer. Each lysate vial contains 0.1 mg lysate in 0.1 ml (1 mg/ml) of RIPA Buffer (50 mM Tris-HCl pH7.5, 250 mM NaCl, 5 mM EDTA, 50 mM NaF, 1% NP40). The loading buffer vial contains 0.5 ml 2X SDS Loading Buffer (125 mM Tris-Cl, pH6.8, 10% glycerol, 4% SDS, 0.002% Bromophenol blue, 5% beta-mercaptoethanol). |
Size : | 0.1 mg |
Storage Instruction : | Store at -80°C. Minimize freeze-thaw cycles. After addition of 2X SDS Loading Buffer, the lysates can be stored at -20°C. Product is guaranteed 6 months from the date of shipment. |
Applications : | ELISA, WB, IP. WB: Mix equal volume of lysates with 2X SDS Loading Buffer. Boil the mixture for 10 min before loading (for membrane protein lysates, incubate the mixture at room temperature for 30 min). Load 5 ug lysate per lane. |
Gene Name : | ANAPC11 anaphase promoting complex subunit 11 [ Homo sapiens ] |
Official Symbol : | ANAPC11 |
Synonyms : | ANAPC11; anaphase promoting complex subunit 11; anaphase promoting complex subunit 11 (yeast APC11 homolog); anaphase-promoting complex subunit 11; APC11; Apc11p; HSPC214; MGC882; cyclosome subunit 11; APC11 anaphase promoting complex subunit 11 homolog; hepatocellular carcinoma-associated RING finger protein; |
Gene ID : | 51529 |
mRNA Refseq : | NM_001002247 |
Protein Refseq : | NP_001002247 |
MIM : | 614534 |
UniProt ID : | Q9NYG5 |
Chromosome Location : | 17q25.3 |
Pathway : | APC/C complex, organism-specific biosystem; APC/C complex, conserved biosystem; APC/C-mediated degradation of cell cycle proteins, organism-specific biosystem; APC/C:Cdc20 mediated degradation of Cyclin B, organism-specific biosystem; APC/C:Cdc20 mediated degradation of Securin, organism-specific biosystem; APC/C:Cdc20 mediated degradation of mitotic proteins, organism-specific biosystem; APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1, organism-specific biosystem; |
Function : | metal ion binding; contributes_to ubiquitin-protein ligase activity; zinc ion binding; |
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Anapc11-1620M | Recombinant Mouse Anapc11 Protein, Myc/DDK-tagged | +Inquiry |
ANAPC11-5685Z | Recombinant Zebrafish ANAPC11 | +Inquiry |
ANAPC11-318R | Recombinant Rhesus monkey ANAPC11 Protein, His-tagged | +Inquiry |
ANAPC11-010H | Recombinant Human ANAPC11 Protein, His-tagged | +Inquiry |
◆ Lysates | ||
ANAPC11-8869HCL | Recombinant Human ANAPC11 293 Cell Lysate | +Inquiry |
ANAPC11-8868HCL | Recombinant Human ANAPC11 293 Cell Lysate | +Inquiry |
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For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (17)
Ask a questionWhile ANAPC11 is best known for its role in cell cycle regulation as a component of the APC/C complex, emerging research suggests that it may have additional functions. For instance, ANAPC11 has been implicated in DNA damage response and repair mechanisms, and it may play a role in chromatin remodeling and gene expression regulation. Further investigations are needed to fully understand these potential non-canonical roles of ANAPC11.
ANAPC11 is primarily localized to the nucleus, specifically in the nucleoplasm, where it associates with other subunits of the APC/C complex. However, in some cases, ANAPC11 can also be detected in the cytoplasm.
The expression of ANAPC11 can be regulated by various factors. For example, studies have shown that the transcription factor E2F1 can directly bind to the ANAPC11 promoter and enhance its expression, thus promoting cell cycle progression. Additionally, microRNAs (miRNAs), such as miR-27a and miR-148a, have been identified as negative regulators of ANAPC11 expression. These miRNAs can directly bind to the ANAPC11 mRNA and inhibit its translation.
Ongoing and future research on ANAPC11 aims to deepen our understanding of its cellular functions and regulatory mechanisms. This includes investigating its roles outside of cell cycle regulation, exploring its interactions with other signaling pathways, and identifying potential therapeutic interventions for diseases associated with ANAPC11 dysregulation. Additionally, further studies may elucidate the precise molecular mechanisms by which ANAPC11 contributes to normal cell cycle progression and cellular homeostasis.
To study ANAPC11, researchers commonly use techniques such as gene expression analysis, protein-protein interaction assays, and functional assays using cell lines or animal models. These methods can help elucidate its role in cell cycle regulation, identify interacting partners, and investigate the effects of ANAPC11 dysregulation. Additionally, gene editing techniques like CRISPR/Cas9 can be employed to manipulate ANAPC11 expression and study its effects on cellular processes.
ANAPC11 has shown potential as a diagnostic and prognostic marker in various types of cancer. Alterations in ANAPC11 expression have been correlated with tumor stage, grade, and patient survival in cancers such as colorectal cancer, breast cancer, and hepatocellular carcinoma.
While ANAPC11's primary role is in the cell cycle as part of the APC/C complex, it also participates in other cellular processes. ANAPC11 is involved in the degradation of proteins associated with DNA replication, centrosome duplication, checkpoint control, and cellular differentiation, indicating its broader role in regulating various cellular events.
ANAPC11 dysregulation has been implicated in various diseases and disorders. For example, alterations in the expression or function of ANAPC11 have been observed in several types of cancer, including colorectal cancer, breast cancer, and hepatocellular carcinoma. Additionally, mutations in ANAPC11 have been linked to developmental disorders such as Cornelia de Lange syndrome and Roberts syndrome.
Targeting the components of the APC/C complex, including ANAPC11, has been explored as a potential strategy for cancer treatment. The APC/C complex dysfunction often leads to defective cell cycle regulation in cancer cells, making it an attractive target for therapy. However, further research is needed to develop specific inhibitors or modulators of ANAPC11 for clinical applications.
Mutations in genes encoding APC/C subunits, including ANAPC11, have been observed in certain cancers. Altered expression or mutations in ANAPC11 have been correlated with tumor progression and poor prognosis in gastric cancer, colorectal cancer, and hepatocellular carcinoma. However, more research is required to establish a direct causative role and understand the underlying mechanisms.
Researchers use various techniques to study the function and regulation of ANAPC11. Common methods include Western blotting, immunoprecipitation, site-directed mutagenesis, siRNA-mediated knockdown, and CRISPR/Cas9 gene editing. Additionally, techniques such as cell cycle analysis, fluorescence microscopy, and biochemical assays are employed to investigate ANAPC11's role in the cell cycle and protein degradation processes.
Studies have shown that depletion of ANAPC11 leads to defects in cell cycle progression, improper chromosome segregation, and accumulation of DNA damage, indicating that ANAPC11 is essential for normal cell viability and division. However, the extent of its indispensability may vary among different cell types and tissues.
ANAPC11 can interact with various proteins and participate in several signaling pathways. For example, it interacts with the spindle assembly checkpoint protein BUB3, regulating the recruitment of BUBR1 to kinetochores during mitosis. ANAPC11 also interacts with the tumor suppressor protein p53, influencing its stability and activity. These interactions suggest a role for ANAPC11 outside of the APC/C complex.
Yes, ANAPC11 is highly conserved across different species. Homologs of ANAPC11 have been identified in various organisms, ranging from yeast to humans. This conservation suggests that ANAPC11 plays a fundamental role in essential cellular processes and highlights its evolutionary significance.
Post-translational modifications (PTMs) of ANAPC11 have not been extensively studied. However, emerging evidence suggests that ANAPC11 may undergo modifications such as phosphorylation and sumoylation. These PTMs can potentially influence the stability, activity, or interaction partners of ANAPC11, thereby modulating its function within the APC/C complex. Future research is needed to fully characterize the PTMs of ANAPC11 and their functional significance.
ANAPC11 protein levels are regulated throughout the cell cycle. Its expression is tightly controlled, with increased levels during the G2/M phase when the APC/C complex is most active. Multiple mechanisms, including transcriptional regulation, protein stabilization, and post-translational modifications such as phosphorylation, are involved in the regulation of ANAPC11.
As of now, there are no specific drugs that target ANAPC11 directly. However, due to the critical role of the APC/C complex in cell cycle regulation and its involvement in various diseases, including cancer, targeting other components of the APC/C complex is an active area of research for developing therapeutic interventions. These efforts may indirectly impact ANAPC11 function.
Customer Reviews (4)
Write a reviewThe technical support provided by the manufacturer is invaluable in overcoming experimental hurdles and optimizing the utilization of ANAPC11 protein.
The ANAPC11 protein offered by the manufacturer is of exceptional quality, making it an ideal choice to fulfill my experimental needs.
Their technical expertise, product quality, customer support, and supply management collectively contribute to the success and progress of my trials.
Its purity, integrity, and functionality are ensured through stringent quality control measures, which instills confidence in the reliability and accuracy of my research results.
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