Antibodies to Cyclin Family - Product Review 16
Introduction
Oscillations in the activity of the Cdk family of protein kinases drive the eukaryotic cell cycle. These enzymes consist of a catalytic (Cdk) and a regulatory subunit (Cyclin).
Their activity is regulated by phosphorylation of Cdks, binding of stoichiometric kinase inhibitors and regulated proteolysis of the cyclins.The Cdk/cyclin family contains five Cdks (Cdk1, 2, 3, 4 and 6) and four cyclin classes (cyclin A, B, D and E, see table below.) that regulate the cell cycle; three Cdks (Cdk7, 8 and 9) and three cyclin classes (cyclin C, H and T) that regulate transcription. Activating the cell-cycle Cdks requires phosphorylation of a conserved threonine as well as binding of cyclin.
Antibody Tools for Detection of Cyclin Proteins
Acris Antibodies offers a broad panel of monoclonal and polyclonal antibodies for the immunological detection of members of the Cyclin protein family.
Picture Gallery
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Available Antibodies to the Cyclin Family
Anti- Cyclin A (CCNA), Cyclin A1 (CCNA1), Cyclin B1 (CCNB), Cyclin B2 (CCNB2), Cyclin B3 (CCNB3), Cyclin C (CCNC), Cyclin D1 (CCND1), Cyclin D2 (CCND2), Cyclin D3 (CCND3), Cyclin E (CCNE), Cyclin E1 (CCNE1), Cyclin E2 (CCNE2), Cyclin G (CCNG), Cyclin G1 (CCNG1), Cyclin G2 (CCNG2), Cyclin H (CCNH), Cyclin I (CCNI), Cyclin J (CCNJ), Cyclin K (CCNK), Cyclin L1 (CCNL1), Cyclin L2 (CCNL2), Cyclin T1 (CCNT1), Cyclin T2 (CCNT2) antibody
Antibodies
| Catalog No. | Host | Clone/Iso. | Pres. | React. | Applications | ||
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| AP12597PU-N |
Cyclin B1 pSer126 antibody | ||||||
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Rabbit | Aff - Purified | Hu | E, P, WB |
0.1 mg /
€330.00
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| Ig | Acris Antibodies GmbH | ||||||
+1 additional image | |||||||
| R1566P |
Cyclin B1 pSer126 antibody | ||||||
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Rabbit | Aff - Purified | Hu | E |
0.1 mg /
€320.00
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| Acris Antibodies GmbH | |||||||





+1 additional image![Figure 1. Western blot using Affinity Purified anti- Cyclin B1
pS126 antibody shows detection of a band ~48 kDa corresponding to
phosphorylated human Cyclin B1 (arrowheads) in various whole cell
lysates. Lysates tested were lane 1 - Hela (cervical carcinoma), lane 2 -
H23 (lung carcinoma), lane 3 - Hep3b (Hepatocarcinoma), lane 4 - T98G
(Glioblastoma) and lane 5 - Daudi (B cell lymphoblast). Each lane
contains approximately 50 µg of lysates, separated by 12% SDS-PAGE
using a 5% stack run at 100 volts until the dye front cleared the bottom of
the gel. Transfer occurred overnight at 4° C at 15 mAmps. The
membrane was blocked with 5% non-fat dry milk in TTBS for 1 h at room
temperature followed by addition of a 1:100 dilution of the antibody
allowed to react for 2h at room temperature. After washes with TTBS a
1:5,000 dilution of HRP conjugated Gt-a-Rabbit IgG [H&L] MX (611-103-
122) was added for 1 h at room temperature. After additional washes the
membrane was incubated with ECL mix 1:1 for ~3 min. Excess detection
solution was drained off and the membrane was exposed to Kodak film
X-omat blue XB-1 for about 20 sec. Other detection systems will yield
similar results. Personnel Communication, Luca Cote, Temple U.](http://m1.acris-antibodies.com/catalog/product/cache/1/small_image/50x50/9df78eab33525d08d6e5fb8d27136e95/0094515.jpeg)