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mCherry Mouse Monoclonal Antibody [A9F2]

RMB: 599 特惠 1500

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Catalog# HA601186

mCherry Mouse Monoclonal Antibody [A9F2]

Application

  • WB

  • IF-Cell

Reactivity

  • Species independent

This product has been cited in peer reviewed publications, see list HERE

概述

产品名称

mCherry Mouse Monoclonal Antibody [A9F2]

抗体类型

Mouse Monoclonal Antibody

免疫原

Recombinant protein within mCherry aa 1-236 / 236.

种属反应性

Species independent

验证应用

WB, IF-Cell

偶联

unconjugated

克隆号

A9F2

RRID

AB_3071905

产品特性

形态

Liquid

浓度

1.17ug/ul

存放说明

Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.

存储缓冲液

PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.

亚型

IgG2b

纯化方式

Protein A affinity purified.

应用稀释度

  • WB

  • 1:2,000-1:5,000

  • IF-Cell

  • 1:2,000

发表文章中的应用

Co-IP 查看 1 篇文献如下

发表文章中的种属

Human 查看 1 篇文献如下

靶点

功能

mCherry is a member of the mFruits family of monomeric red fluorescent proteins (mRFPs). As a RFP, mCherry was derived from DsRed of Discosoma sea anemones unlike green fluorescent proteins (GFPs) which are often derived from Aequoera victoria jellyfish.Fluorescent proteins are used to tag components in the cell, so they can be studied using fluorescence spectroscopy and fluorescence microscopy. mCherry absorbs light between 540-590 nm and emits light in the range of 550-650 nm. mCherry belongs to the group of fluorescent protein chromophores used as instruments to visualize genes and analyze their functions in experiments. Genome editing has been improved greatly through the precise insertion of these fluorescent protein tags into the genetic material of many diverse organisms. Most comparisons between the brightness and photostability of different fluorescent proteins have been made in vitro, removed from biological variables that affect protein performance in cells or organisms. It is hard to perfectly simulate cellular environments in vitro, and the difference in environment could have an effect on the brightness and photostability.

背景文献

1. Sun J et al. A Glb1-2A-mCherry reporter monitors systemic aging and predicts lifespan in middle-aged mice. Nat Commun. 2022 Nov

2. Langa S et al. Evoglow-Pp1 and mCherry proteins: a dual fluorescent labeling system for lactic acid bacteria. Appl Microbiol Biotechnol. 2021 Oct

UNIPROT

SwissProt: X5DSL3 AnaplasmaMarginale

图片

  • <span style="font-weight: bold;">☑ Cell treatment (CT)</span><br /><br />Western blot analysis of mCherry on different lysates with Mouse anti-mCherry antibody (<a href="/products/HA601186" style="font-weight: bold;text-decoration: underline;">HA601186</a>) at 1/2,000 dilution.<br /><br />Lane 1: 293T-WT cell lysate (5 µg/Lane)<br />Lane 2: 293T-OE-mCherry cell lysate (5 µg/Lane)<br />Lane 3: 293T-OE-mCherry cell lysate (2.5 µg/Lane)<br />Lane 4: 293T-OE-mCherry cell lysate (1.25 µg/Lane)<br />Lane 5: 293T-OE-mCherry cell lysate (0.625 µg/Lane)<br /><br />Predicted band size: 27 kDa<br />Observed band size: 27 kDa<br /><br />Exposure time: 30 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/HA601186" style="font-weight: bold;text-decoration: underline;">HA601186</a>) at 1/2,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (<a href="/products/HA1006" style="font-weight: bold;text-decoration: underline;">HA1006</a>) at 1/150,000 dilution was used for 1 hour at room temperature.

    ☑ Cell treatment (CT)

    Western blot analysis of mCherry on different lysates with Mouse anti-mCherry antibody (HA601186) at 1/2,000 dilution.

    Lane 1: 293T-WT cell lysate (5 µg/Lane)
    Lane 2: 293T-OE-mCherry cell lysate (5 µg/Lane)
    Lane 3: 293T-OE-mCherry cell lysate (2.5 µg/Lane)
    Lane 4: 293T-OE-mCherry cell lysate (1.25 µg/Lane)
    Lane 5: 293T-OE-mCherry cell lysate (0.625 µg/Lane)

    Predicted band size: 27 kDa
    Observed band size: 27 kDa

    Exposure time: 30 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 (HA601186) at 1/2,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1/150,000 dilution was used for 1 hour at room temperature.

  • Western blot analysis of mCherry on mCherry recombinant protein with Mouse anti-mCherry antibody (<a href="/products/HA601186" style="font-weight: bold;text-decoration: underline;">HA601186</a>) at 1/1,000 dilution.<br /><br />Lane 1: mCherry recombinant protein, 500ng/Lane<br />Lane 2: mCherry recombinant protein, 250ng/Lane<br />Lane 3: mCherry recombinant protein, 125ng/Lane<br />Lane 4: mCherry recombinant protein, 62.5ng/Lane<br /><br />Exposure time: 30 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/HA601186" style="font-weight: bold;text-decoration: underline;">HA601186</a>) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (<a href="/products/HA1006" style="font-weight: bold;text-decoration: underline;">HA1006</a>) at 1/150,000 dilution was used for 1 hour at room temperature.

    Western blot analysis of mCherry on mCherry recombinant protein with Mouse anti-mCherry antibody (HA601186) at 1/1,000 dilution.

    Lane 1: mCherry recombinant protein, 500ng/Lane
    Lane 2: mCherry recombinant protein, 250ng/Lane
    Lane 3: mCherry recombinant protein, 125ng/Lane
    Lane 4: mCherry recombinant protein, 62.5ng/Lane

    Exposure time: 30 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 (HA601186) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1/150,000 dilution was used for 1 hour at room temperature.

  • Western blot analysis of mCherry on different lysates with Mouse anti-mCherry antibody (<a href="/products/HA601186" style="font-weight: bold;text-decoration: underline;">HA601186</a>) at 1/5,000 dilution.<br /><br />Lane 1: 293T cell lysate<br />Lane 2: 293T transfected with mCherry-tagged cell lysate<br />Lane 3: 293T transfected with GFP-tagged cell lysate (negative)<br /><br />Lysates/proteins at 5 µg/Lane.<br /><br />Exposure time: 3 minutes; ECL: K1801;<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/HA601186" style="font-weight: bold;text-decoration: underline;">HA601186</a>) at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody (<a href="/products/HA1006" style="font-weight: bold;text-decoration: underline;">HA1006</a>) at 1/50,000 dilution was used for 1 hour at room temperature.

    Western blot analysis of mCherry on different lysates with Mouse anti-mCherry antibody (HA601186) at 1/5,000 dilution.

    Lane 1: 293T cell lysate
    Lane 2: 293T transfected with mCherry-tagged cell lysate
    Lane 3: 293T transfected with GFP-tagged cell lysate (negative)

    Lysates/proteins at 5 µg/Lane.

    Exposure time: 3 minutes; ECL: K1801;

    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 (HA601186) at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1/50,000 dilution was used for 1 hour at room temperature.

  • Immunocytochemistry analysis of 293T transfected with or without mCherry cells labeling mCherry with Mouse anti-mCherry antibody (<a href="/products/HA601186" style="font-weight: bold;text-decoration: underline;">HA601186</a>) at 1/2,000 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 Mouse anti-mCherry antibody (<a href="/products/HA601186" style="font-weight: bold;text-decoration: underline;">HA601186</a>) at 1/2,000 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Mouse IgG H&L (iFluor&trade; 488, <a href="/products/HA1125" style="font-weight: bold;text-decoration: underline;">HA1125</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. As expected, green antibody staining is only visible in cells expressing mCherry, and green and red signals can be superimposed.

    Immunocytochemistry analysis of 293T transfected with or without mCherry cells labeling mCherry with Mouse anti-mCherry antibody (HA601186) at 1/2,000 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 Mouse anti-mCherry antibody (HA601186) at 1/2,000 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Mouse IgG H&L (iFluor™ 488, HA1125) 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. As expected, green antibody staining is only visible in cells expressing mCherry, and green and red signals can be superimposed.

请注意: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

引文

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