CNOT7 Recombinant Rabbit Monoclonal Antibody [PSH02-81]
cat.: HA721861
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, FC
Clonality: Monoclonal
Clone number: PSH02-81
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 33 kDa
Isotype: IgG
Immunogen: Recombinant protein within human CNOT7 aa 1-285 / 285.
Positive control: HeLa cell lysate, HepG2 cell lysate, NCCIT cell lysate, Jurkat cell lysate, THP-1 cell lysate, mouse brain tissue lysate, rat spleen tissue lysate, F9.
Subcellular location: Nucleus, Cytoplasm, P-body, Cytoplasmic ribonucleoprotein granule.
Recommended Dilutions:
  WB
  IF-Cell
  FC

1:2,000
1:100
1:1,000
Uniprot #: SwissProt: Q9UIV1 Human | Q60809 Mouse
Entrez Gene: 306492 Rat
Alternative names: BTG1 binding factor 1 BTG1-binding factor 1 CAF 1 CAF-1 CAF1 Carbon catabolite repressor protein (CCR4) associative factor 1 CCR4 associated factor 1 CCR4 NOT transcription complex subunit 7 CCR4-associated factor 1 CCR4-NOT transcription complex subunit 7 CNOT 7 Cnot7 CNOT7_HUMAN hCAF 1 hCAF1
Images
HA721861_1.jpg Fig1: Western blot analysis of CNOT7 on different lysates with Rabbit anti-CNOT7 antibody (HA721861) at 1/2,000 dilution.

Lane 1: HeLa cell lysate (20 µg/Lane)
Lane 2: HepG2 cell lysate (20 µg/Lane)
Lane 3: NCCIT cell lysate (20 µg/Lane)
Lane 4: Jurkat cell lysate (20 µg/Lane)
Lane 5: THP-1 cell lysate (20 µg/Lane)
Lane 6: Mouse brain tissue lysate (40 µg/Lane)
Lane 7: Rat spleen tissue lysate (40 µg/Lane)

Predicted band size: 33 kDa
Observed band size: 33 kDa

Exposure time: 3 minutes 20 seconds;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721861) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
HA721861_2.jpg Fig2: Immunocytochemistry analysis of F9 cells labeling CNOT7 with Rabbit anti-CNOT7 antibody (HA721861) at 1/200 dilution.

Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-CNOT7 antibody (HA721861) at 1/200 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
HA721861_3.jpg Fig3: Flow cytometric analysis of F9 cells labeling CNOT7.

Cells were fixed and permeabilized. Then stained with the primary antibody (HA721861, 1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.