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KD-Validated CINP Mouse mAb (20 μl)

$149.00

Cat. #: 63833

Description

Reactivity: Human
Applications: WB, FC
Host Species: Mouse
Isotype: IgG2b
Clonality: Monoclonal antibody
Gene Name: cyclin dependent kinase 2 interacting protein
Gene Symbol: CINP
Gene ID: 51550
UniProt ID: Q9BW66
Clone ID: 24GB8100
Immunogen: Recombinant protein of human CINP
Dilution: WB 1:500-1:2,500; FC 1:2,000
Purification Method: Affinity purified
Concentration: Lot dependent
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Storage: Store at -20°C. Avoid freeze/thaw cycles.


Background

The protein encoded by this gene is reported to be a component of the DNA replication complex as well as a genome-maintenance protein. It may interact with proteins important for replication initiation and has been shown to bind chromatin at the G1 phase of the cell cycle and dissociate from chromatin with replication initiation. It may also serve to regulate checkpoint signaling as part of the DNA damage response. Alternative splicing results in multiple transcript variants.


Images

CINP antibody Western blotting analysis using anti-CINP antibody (Cat#63833). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-CINP antibody (Cat#63833, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
63833 WB KD 1 Western blotting analysis using anti-CINP antibody (Cat#63833). CINP expression in wild type (WT) and CINP shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-CINP antibody (Cat#63833, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
63833 FCM 1 Flow cytometric analysis of CINP expression in HepG2 cells using anti-CINP antibody (Cat#63833, 1:2,000). Green, isotype control; red, CINP.


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