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CNOT7 Recombinant Rabbit Monoclonal Antibody [PSH02-81] - BSA and Azide free

Usd: 649

Specification

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Catalog# HA750836

CNOT7 Recombinant Rabbit Monoclonal Antibody [PSH02-81] - BSA and Azide free

Application

  • WB

  • IF-Cell

  • FC

Reactivity

  • Human

  • Mouse

  • Rat

With BSA and Azide
Conjugation

  • unconjugated

Overview

Product Name

CNOT7 Recombinant Rabbit Monoclonal Antibody [PSH02-81] - BSA and Azide free

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Recombinant protein within human CNOT7 aa 1-285 / 285.

Species Reactivity

Human, Mouse, Rat

Validated Applications

WB, IF-Cell, FC

Target Molecular Weight

Predicted band size: 33 kDa

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.

Conjugation

unconjugated

Clone Number

PSH02-81

Product Features

Form

Liquid

Concentration

1mg/ml

Storage Instructions

Store at 2-8℃. Avoid freeze.

Storage Buffer

1*PBS (pH7.4).

Isotype

IgG

Purification Method

Protein A affinity purified.

Application Dilution

Target

Function

The protein encoded by this gene binds to an anti-proliferative protein, B-cell translocation protein 1, which negatively regulates cell proliferation. Binding of the two proteins, which is driven by phosphorylation of the anti-proliferative protein, causes signaling events in cell division that lead to changes in cell proliferation associated with cell-cell contact. The encoded protein downregulates the innate immune response and therefore provides a therapeutic target for enhancing its antimicrobial activity against foreign agents. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1 and X.

Background References

1. Yu J et al. CNOT7 modulates biological functions of ovarian cancer cells via AKT signaling pathway. Life Sci. 2021 Mar

2. Stoney PN et al. CNOT7 Outcompetes Its Paralog CNOT8 for Integration into The CCR4-NOT Complex. J Mol Biol. 2022 May

Subcellular Location

Nucleus, Cytoplasm, P-body, Cytoplasmic ribonucleoprotein granule.

UNIPROT

SwissProt: Q9UIV1 Human

SwissProt: Q60809 Mouse

Entrez Gene: 306492 Rat

Synonyms

BTG1 binding factor 1 antibody

BTG1-binding factor 1 antibody

CAF 1 antibody

CAF-1 antibody

CAF1 antibody

Carbon catabolite repressor protein (CCR4) associative factor 1 antibody

CCR4 associated factor 1 antibody

CCR4 NOT transcription complex subunit 7 antibody

CCR4-associated factor 1 antibody

CCR4-NOT transcription complex subunit 7 antibody

Expand

Images

  • This data was developed using <a href="/products/HA721861" style="font-weight: bold;text-decoration: underline;">HA721861</a>, the same antibody clone in a different buffer formulation.<br />Western blot analysis of CNOT7 on different lysates with Rabbit anti-CNOT7 antibody (<a href="/products/HA721861" style="font-weight: bold;text-decoration: underline;">HA721861</a>) at 1/2,000 dilution.<br /><br />Lane 1: HeLa cell lysate (20 µg/Lane)<br />Lane 2: HepG2 cell lysate (20 µg/Lane)<br />Lane 3: NCCIT cell lysate (20 µg/Lane)<br />Lane 4: Jurkat cell lysate (20 µg/Lane)<br />Lane 5: THP-1 cell lysate (20 µg/Lane)<br />Lane 6: Mouse brain tissue lysate (40 µg/Lane)<br />Lane 7: Rat spleen tissue lysate (40 µg/Lane)<br /><br />Predicted band size: 33 kDa<br />Observed band size: 33 kDa<br /><br />Exposure time: 3 minutes 20 seconds;<br /><br />4-20% SDS-PAGE gel.<br /><br />Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (<a href="/products/HA721861" style="font-weight: bold;text-decoration: underline;">HA721861</a>) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (<a href="/products/HA1001" style="font-weight: bold;text-decoration: underline;">HA1001</a>) at 1/50,000 dilution was used for 1 hour at room temperature.

    This data was developed using HA721861, the same antibody clone in a different buffer formulation.
    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.

  • This data was developed using <a href="/products/HA721861" style="font-weight: bold;text-decoration: underline;">HA721861</a>, the same antibody clone in a different buffer formulation.<br />Immunocytochemistry analysis of F9 cells labeling CNOT7 with Rabbit anti-CNOT7 antibody (<a href="/products/HA721861" style="font-weight: bold;text-decoration: underline;">HA721861</a>) at 1/200 dilution.<br /><br />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 (<a href="/products/HA721861" style="font-weight: bold;text-decoration: underline;">HA721861</a>) at 1/200 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor&trade; 488, <a href="/products/HA1121" style="font-weight: bold;text-decoration: underline;">HA1121</a>) 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.<br /><br />Beta tubulin (<a href="/products/M1305-2" style="font-weight: bold;text-decoration: underline;">M1305-2</a>, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor&trade; 594, <a href="/products/HA1126" style="font-weight: bold;text-decoration: underline;">HA1126</a>) was used as the secondary antibody at 1/1,000 dilution.

    This data was developed using HA721861, the same antibody clone in a different buffer formulation.
    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.

  • This data was developed using <a href="/products/HA721861" style="font-weight: bold;text-decoration: underline;">HA721861</a>, the same antibody clone in a different buffer formulation.<br />Flow cytometric analysis of F9 cells labeling CNOT7.<br /><br />Cells were fixed and permeabilized. Then stained with the primary antibody (<a href="/products/HA721861" style="font-weight: bold;text-decoration: underline;">HA721861</a>, 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&trade; 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (<a href="/products/HA1121" style="font-weight: bold;text-decoration: underline;">HA1121</a>) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

    This data was developed using HA721861, the same antibody clone in a different buffer formulation.
    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).

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