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GFP Recombinant Rabbit Monoclonal Antibody [SY0243]

RMB: 599 特惠 1500

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Catalog# ET1607-31

GFP Recombinant Rabbit Monoclonal Antibody [SY0243]

Application

  • WB

  • IF-Cell

  • IF-Tissue

  • IP

  • IHC-P

Reactivity

  • Species independent

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

概述

产品名称

GFP Recombinant Rabbit Monoclonal Antibody [SY0243]

抗体类型

Recombinant Rabbit monoclonal Antibody

免疫原

Synthetic peptide within Aequorea victoria GFP aa 1-50 / 238.

种属反应性

Species independent

验证应用

WB, IF-Cell, IF-Tissue, IP, IHC-P

分子量

Predicted band size: 27 kDa

阳性对照

GFP recombinant protein.

偶联

unconjugated

克隆号

SY0243

RRID

AB_3069758

产品特性

形态

Liquid

浓度

1ug/ul

存放说明

Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.

存储缓冲液

1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.

亚型

IgG

纯化方式

Protein A affinity purified.

应用稀释度

  • WB

  • 1:10,000

  • IF-Cell

  • 1:50-1:200

  • IF-Tissue

  • 1:50-1:200

  • IP

  • 2-5 µg/ml.

  • IHC-P

  • 1:5,000

发表文章中的种属

Human See 9 publications below
Magnaporthe oryzae See 3 publications below
Zebrafish See 2 publications below

靶点

功能

The green fluorescent protein (GFP) was originally identified as a protein involved in the bioluminescence of the jellyfish Aequorea victoria. GFP cDNA produces a fluorescent product when expressed in prokaryotic cells, without the need for exogenous substrates or cofactors, making GFP a useful tool for monitoring gene expression and protein localization in vivo. Several GFP mutants have been developed, including EGFP, which fluoresce more intensely than the wildtype GFP and have shifted excitation maxima, making them useful for FACS and fluorescence microscopy as well as double-labeling applications. GFP is widely used in expression vectors as a fusion protein tag, allowing expression and monitoring of heterologous proteins fused to GFP.

背景文献

1. Yu, H. et al. 2016. AAV-Mediated Gene Transfer to Dorsal Root Ganglion. Methods in molecular biology (Clifton, N.J.). 1382: 251-61.

2. Yamaoka, M. et al. 2016. PI3K regulates endocytosis after insulin secretion by mediating signaling crosstalk between Arf6 and Rab27a. J. Cell. Sci. 129: 637-49.

UNIPROT #

SwissProt: P42212 AequoreaVictoria

别名

GFP antibody

Green fluorescent protein antibody

yfp antibody

图片

  • Western blot analysis of GFP on GFP recombinant protein with Rabbit anti-GFP antibody (<a href="/products/ET1607-31" style="font-weight: bold;text-decoration: underline;">ET1607-31</a>) at 1/10,000 dilution.<br /><br />Lysates/proteins at 50 ng/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/ET1607-31" style="font-weight: bold;text-decoration: underline;">ET1607-31</a>) at 1/10,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (<a href="/products/HA1001" style="font-weight: bold;text-decoration: underline;">HA1001</a>) at 1:100,000 dilution was used for 1 hour at room temperature.

    Western blot analysis of GFP on GFP recombinant protein with Rabbit anti-GFP antibody (ET1607-31) at 1/10,000 dilution.

    Lysates/proteins at 50 ng/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 (ET1607-31) at 1/10,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:100,000 dilution was used for 1 hour at room temperature.

  • GFP tag was immunoprecipitated in 5µg GFP Tag fusion protein lysate with <a href="/products/ET1607-31" style="font-weight: bold;text-decoration: underline;">ET1607-31</a> at 2 µg/20 µl agarose. Western blot was performed from the immunoprecipitate using <a href="/products/M1004-8" style="font-weight: bold;text-decoration: underline;">M1004-8</a> at 1/1000 dilution. Anti-Mouse IgG - HRP Secondary Antibody (<a href="/products/HA1006" style="font-weight: bold;text-decoration: underline;">HA1006</a>) at 1:20,000 dilution was used for 60 mins at room temperature.<br /><br />Lane 1: GFP Tag fusion protein lysate (input).<br />Lane 2: Rabbit IgG instead of <a href="/products/ET1607-31" style="font-weight: bold;text-decoration: underline;">ET1607-31</a> in GFP Tag fusion protein lysate.<br />Lane 3: <a href="/products/ET1602-7" style="font-weight: bold;text-decoration: underline;">ET1602-7</a> IP in GFP Tag fusion protein lysate.<br />Lane 4: <a href="/products/ET1604-25" style="font-weight: bold;text-decoration: underline;">ET1604-25</a> IP in GFP Tag fusion protein lysate.<br />Lane 5: <a href="/products/ET1604-26" style="font-weight: bold;text-decoration: underline;">ET1604-26</a> IP in GFP Tag fusion protein lysate.<br />Lane 6: <a href="/products/ET1607-31" style="font-weight: bold;text-decoration: underline;">ET1607-31</a> IP in GFP Tag fusion protein lysate.<br />Lane 7: <a href="/products/R1312-2" style="font-weight: bold;text-decoration: underline;">R1312-2</a> IP in GFP Tag fusion protein lysate.<br /><br />Blocking/Dilution buffer: 5% NFDM/TBST

    GFP tag was immunoprecipitated in 5µg GFP Tag fusion protein lysate with ET1607-31 at 2 µg/20 µl agarose. Western blot was performed from the immunoprecipitate using M1004-8 at 1/1000 dilution. Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1:20,000 dilution was used for 60 mins at room temperature.

    Lane 1: GFP Tag fusion protein lysate (input).
    Lane 2: Rabbit IgG instead of ET1607-31 in GFP Tag fusion protein lysate.
    Lane 3: ET1602-7 IP in GFP Tag fusion protein lysate.
    Lane 4: ET1604-25 IP in GFP Tag fusion protein lysate.
    Lane 5: ET1604-26 IP in GFP Tag fusion protein lysate.
    Lane 6: ET1607-31 IP in GFP Tag fusion protein lysate.
    Lane 7: R1312-2 IP in GFP Tag fusion protein lysate.

    Blocking/Dilution buffer: 5% NFDM/TBST

  • Immunocytochemistry analysis of HeLa cells transfected with N-terminal GFP labeling GFP with Rabbit anti-GFP antibody (<a href="/products/ET1607-31" style="font-weight: bold;text-decoration: underline;">ET1607-31</a>) at 1/500 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-GFP antibody (<a href="/products/ET1607-31" style="font-weight: bold;text-decoration: underline;">ET1607-31</a>) at 1/500 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor&trade; 594, <a href="/products/HA1122" style="font-weight: bold;text-decoration: underline;">HA1122</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. Counterstained with GFP (green). Nuclear DNA was labelled in blue with DAPI.

    Immunocytochemistry analysis of HeLa cells transfected with N-terminal GFP labeling GFP with Rabbit anti-GFP antibody (ET1607-31) at 1/500 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-GFP antibody (ET1607-31) at 1/500 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 594, HA1122) 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. Counterstained with GFP (green). Nuclear DNA was labelled in blue with DAPI.

  • Immunohistochemical analysis of paraffin-embedded mouse brain tissue transfected with GFP-tagged CX3CR1 with Rabbit anti-GFP antibody (<a href="/products/ET1607-31" style="font-weight: bold;text-decoration: underline;">ET1607-31</a>) at 1/5,000 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/ET1607-31" style="font-weight: bold;text-decoration: underline;">ET1607-31</a>) at 1/5,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    Immunohistochemical analysis of paraffin-embedded mouse brain tissue transfected with GFP-tagged CX3CR1 with Rabbit anti-GFP antibody (ET1607-31) at 1/5,000 dilution.

    The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1607-31) at 1/5,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • Immunohistochemical analysis of paraffin-embedded mouse brain tissue transfected with GFP-tagged CX3CR1 with Rabbit anti-GFP antibody (<a href="/products/ET1607-31" style="font-weight: bold;text-decoration: underline;">ET1607-31</a>) at 1/5,000 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/ET1607-31" style="font-weight: bold;text-decoration: underline;">ET1607-31</a>) at 1/5,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    Immunohistochemical analysis of paraffin-embedded mouse brain tissue transfected with GFP-tagged CX3CR1 with Rabbit anti-GFP antibody (ET1607-31) at 1/5,000 dilution.

    The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1607-31) at 1/5,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

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

引文

Filter:
  1. WB
  2. Co-IP
  3. IF-cell
  4. IP
  5. co-IP
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