A 1:250 dilution of SPC-937 was sufficient for detection of CDK1 (pThr161) in 10 µg of HeLa cell lysate by ECL immunoblot analysis using goat anti-rabbit IgG:HRP as the secondary antibody.
Biological Description
Alternative Names
Cdc2 Antibody, CDC28A Antibody, CDK 1 Antibody, CDKN1 Antibody, Cell division control protein 2 Antibody, Cell division protein kinase 1 Antibody, Cyclin-dependent kinase 1 Antibody, p34 Cdk1 Antibody, P34CDC2 Antibody
Research Areas
Cancer, Cell Cycle, Cell Signaling, Epigenetics and Nuclear Signaling, Neurodegeneration, Neuroscience, Protein Phosphorylation
Cellular Localization
Nucleus
Accession Number
NP_001777
Gene ID
983
Swiss Prot
P06493
Scientific Background
CDK1 is a protein-serine/threonine kinase. The near absence of reported somatic mutations in this protein indicates that it may function as a tumour requiring protein (TRP) in many human tumours.
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Biotin
Properties:
Binds tetrameric avidin proteins including Streptavidin and neuravidin with very high affinity
Molar mass: 244.31 g/mol
Formula: C10H16N2O3S
Applications: Western blot, immunohistochemistry, and ELISA
① 电泳分离4种核苷酸时应取pH3.5 的缓冲液，在该pH时，这4种单核苷酸之间所带负电荷差异较大，它们都向正极移动，但移动的速度不同，依次为：UMP>GMP>AMP>CMP； ② 应取pH8.0，这样可使核苷酸带较多负电荷，利于吸附于阴离子交换树脂柱。虽然pH 11.4时核苷酸带有更多的负电荷，但pH过高对分离不利。 ③ 当不考虑树脂的非极性吸附时，根据核苷酸负电荷的多少来决定洗脱速度，则洗脱顺序为CMP>AMP> GMP > UMP，但实际上核苷酸和聚苯乙烯阴离子交换树脂之间存在着非极性吸附，嘌呤碱基的非极性吸附是嘧啶碱基的3倍。静电吸附与非极性吸附共同作用的结果使洗脱顺序为：CMP> AMP > UMP >GMP。
