Alternatives Western Blotting (WB), Immunoprecipitation (IP)
|3 references available|
|Price||Product not available in this region.|
|Immunogen||Human APC2 peptide|
|Description||Cell cycle progression through mitosis is regulated in part by controlling the synthesis and degradation of specific cyclins and kinases. Initiation of mitosis occurs when cyclin B and Cdc2 form a complex, causing the phosphorylation of a number of proteins by Cdc2 to initiate the M phase. Cdc2 activation leads to the degradation of cyclin B via an ubiquitin-mediated proteolysis pathway which leads to the inactivation of Cdc2. The initiation of anaphase and exit from mitosis depend on the activation of the anaphase promoting complex (APC), which is composed of proteins responsible for the ubiquitination of anaphase inhibitors and mitotic cyclins. The vertebrate APC has been shown to consist of at least 12 subunits, and APC-2 is one of these subunits. APC2 contains a 200 amino acid residue region, designated the CH region, which has homology to a region in the cullin family of proteins. Cullin proteins function to ubiquinate many phosphorylated substrate proteins, such as cyclin G1. Thus, both APC2 and cullin proteins may perform similar biochemical roles in their respective proteolytic pathways. Human APC2 has been cloned and has an expected molecular weight of ~85 kDa in SDS/PAGE. The antibodies recognize human and mouse APC2. A peptide coupled to KLH and made against the C-terminus of human APC2 (CYSAGVYRLPKNCS) was used as immunogen.|
1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
2. Please refer to us for technical protocols.
3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
|Molecular Weight||85 kDa|
Related Products: ABIN967390, ABIN968538
|Application Notes||Applications include immunoprecipitation (1-3 µl/1x10^6 cells) and western blot analysis (1:2000). NIH/3T3 (ATCC CRL-1658) or HeLa (ATCC CCL-2) cells are recommended as a positive control.|
|Purification||Purified from antiserum by negative adsorption and affinity chromatography.|
|Buffer||Aqueous buffered solution.|
|Preservative||0.09% Sodium azide.|
|Storage||Store undiluted at 4°C.|
|Research Area||Chromatin and Nuclear Signaling, Transcription Factors, Coagulation|
|Restrictions||For Research Use only|
Kipreos, Lander, Wing et al.: "cul-1 is required for cell cycle exit in C. elegans and identifies a novel gene family." in: Cell, Vol. 85, Issue 6, pp. 829-39, 1996 (PubMed).
Zachariae, Shevchenko, Andrews et al.: "Mass spectrometric analysis of the anaphase-promoting complex from yeast: identification of a subunit related to cullins." in: Science (New York, N.Y.), Vol. 279, Issue 5354, pp. 1216-9, 1998 (PubMed).
Yu, Peters, King et al.: "Identification of a cullin homology region in a subunit of the anaphase-promoting complex." in: Science (New York, N.Y.), Vol. 279, Issue 5354, pp. 1219-22, 1998 (PubMed).
|Reactivities||Human (15), Mouse (Murine) (3)|
|Applications||Western Blotting (WB) (15), ELISA (8), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)) (4), Immunocytochemistry (ICC) (3), Immunofluorescence (IF) (1), Immunohistochemistry (IHC) (1), Immunoprecipitation (IP) (1)|
|Epitopes||C-Term (2), Internal Region (2), AA 810-822,C-Term (1), Middle Region (1), N-Term (1)|