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Purified anti-APC1 Antibody
Purified anti-APC1 Antibody
610701 50 µl (5 Western blots) ¥15,000     
610702 200 µl (20 Western blots) ¥45,000     

Product Details

Clone: Poly6107
Isotype: Rabbit IgG
Reactivity: Human
Immunogen: Recombinant (partial), N-terminal
Formulation: This antibody is provided in phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and 50% glycerol.
Preparation: The antibody was purified by antigen-affinity chromatography.
Storage & Handling: Upon receipt, store frozen at -20° C.
Application:

WB - Quality tested

Recommended Usage: Each lot of this antibody is quality control tested by Western blotting. Western blotting, suggested working dilution(s): Use 10 µl per 5 ml antibody dilution buffer for each mini-gel. It is recommended that the reagent be titrated for optimal performance for each application.
COA:
Enter Lot#:   
Jurkat nuclear extract was resolved
Jurkat nuclear extract was resolved by electrophoresis, transferred to nitrocellulose and probed with anti-APC1 antibody. Proteins were visualized using a donkey anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system.


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Description: APC1 (anaphase-promoting complex subunit 1) is a meiotic checkpoint regulator that is a member of the E3 enzyme family. This protein contains Rpn1/2 repeats and has a molecular weight of approximately 216 kD. The APC1 protein is located in the nucleus during interphase, and at the centrosome during metaphase/anaphase. This protein comprises one subunit of the anaphase promoting complex including APC1-8, and other probable complex proteins APC9-11, Cdc26, Mnd2, Swm1. The APC1 protein functions as a probable scaffold for complex assembly, a multisubunit cell cycle ubiquitin ligase, and a regulator of sister chromatid separation by degrading securins. In addition, this protein functions in ubiquitin-dependent cyclin catabolism, metaphase/anaphase transition, and spindle elongation. The APC complex is inactivated by protein kinase A and is activated by CDC20 and Cdh1. The APC1 protein is phosphorylated by Cdk1-cyclin B and can also be ubiquitinated and targeted for degradation. The Poly6017 antibody has been shown to be useful for Western blotting of the human APC1 protein.
Other Names: Anaphase-promoting complex subunit 1, Meiotic checkpoint regulator (MCPR), BimE, Cut4
Structure: E3 enzyme family, Rpn1/2 repeats; 216 kD
Distribution: Nuclear during interphase, centrosome during metaphase/anaphase
Function: Probable scaffold for complex assembly, multisubunit cell cycle ubiquitin ligase. Regulates sister chromatid separation by degrading securins. Involved in ubiquitin-dependent cyclin catabolism, metaphase/anaphase transition, spindle elongation
Regulation: Complex inactivated by protein kinase A (PKA) pathway. Activated by CDC20, Cdh1
Modification: Phosphorylation by Cdk1-cyclin B, Ubiquitination
Interaction: Anaphase promoting complex composed of eight protein subunits APC1-8, APC9-11, Cdc26, Mnd2, and Swm1
Antigen
References:
1. Zachariae W, et al. 1999. Genes Dev. 13:2039.
2. Jorgensen P, et al. 2001. Gene 262:51.
3. Golan A, et al. 2002. J. Biol. Chem. 277:15552.
4. Hall M, et al. 2003. J. Biol. Chem. 278:16698.
GeneID: 324
Latest Publications: View the latest APC1 articles on HighwirePress.com
UniProt: View information about APC1 on UniProt.org
Keywords: Purified anti-APC1, Poly6107, Purified, Anaphase-promoting complex subunit 1, Meiotic checkpoint regulator (MCPR), BimE, Cut4, Human, Immunology, Antibodies
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This data display is provided for general comparisons between formats. Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors. If you need assistance with selecting the best format contact our expert technical support team.

  • Purified anti-APC1
    Jurkat nuclear extract was resolved

    Jurkat nuclear extract was resolved by electrophoresis, transferred to nitrocellulose and probed with anti-APC1 antibody. Proteins were visualized using a donkey anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system.

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