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FXR1 Recombinant Rabbit Monoclonal Antibody [PSH01-35]

RMB: 699 特惠 1500

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Catalog# HA721669

FXR1 Recombinant Rabbit Monoclonal Antibody [PSH01-35]

Application

  • WB

  • IHC-P

  • IF-Cell

  • IP

Reactivity

  • Human

  • Mouse

  • Rat

  • Monkey

BSA and Azide free
Conjugation

  • unconjugated

概述

产品名称

FXR1 Recombinant Rabbit Monoclonal Antibody [PSH01-35]

抗体类型

Recombinant Rabbit monoclonal Antibody

免疫原

Recombinant protein within human FXR1 aa 1-150 / 621.

种属反应性

Human, Mouse, Rat, Monkey

验证应用

WB, IHC-P, IF-Cell, IP

分子量

Predicted band size: 70 kDa

阳性对照

HeLa cell lysate, 293T cell lysate, HepG2 cell lysate, A549 cell lysate, K-562 cell lysate, COS-1 cell lysate, NIH/3T3 cell lysate, C2C12 cell lysate, PC-12 cell lysate, human testis tissue, mouse brain tissue, rat brain tissue, PC-12.

偶联

unconjugated

克隆号

PSH01-35

RRID

AB_3072782

反应性数据

WB IHC-P IF-Cell IP
Human
Tested Tested
Tested Tested
Tested Tested
Mouse
Tested Tested
Tested Tested
Tested Tested
Rat
Tested Tested
Tested Tested
Tested Tested
Monkey
Tested Tested

产品特性

形态

Liquid

浓度

存放说明

Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.

存储缓冲液

PBS (pH7.4), 0.1% 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

  • 1:1,000

  • IHC-P

  • 1:200

  • IF-Cell

  • 1:100

靶点

功能

Fragile X mental retardation syndrome-related protein 1 is a protein that in humans is encoded by the FXR1 gene. The protein encoded by this gene is an RNA binding protein that interacts with the functionally similar proteins FMR1 and FXR2. These proteins shuttle between the nucleus and cytoplasm and associate with polyribosomes, predominantly with the 60S ribosomal subunit. Three transcript variants encoding different isoforms have been found for this gene.

背景文献

1. Kang JY et al. LLPS of FXR1 drives spermiogenesis by activating translation of stored mRNAs. Science. 2022 Aug

2. Khlghatyan J et al. Fxr1 regulates sleep and synaptic homeostasis. EMBO J. 2020 Nov

亚细胞定位

Cytoplasm, Cytoplasmic ribonucleoprotein granule, Stress granule, Cell projection, dendrite, dendritic spine, axon, Nucleus envelope, Postsynapse.

UNIPROT

SwissProt: P51114 Human

SwissProt: Q61584 Mouse

SwissProt: Q5XI81 Rat

别名

Fragile X mental retardation autosomal homolog 1 antibody

Fragile X mental retardation syndrome related protein 1 antibody

Fragile X mental retardation syndrome-related protein 1 antibody

FXR1 antibody

FXR1_HUMAN antibody

FXR1P antibody

hFXR1p antibody

图片

  • Western blot analysis of FXR1 on different lysates with Rabbit anti-FXR1 antibody (<a href="/products/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a>) at 1/1,000 dilution.<br /><br />Lane 1: HeLa cell lysate<br />Lane 2: 293T cell lysate<br />Lane 3: HepG2 cell lysate<br />Lane 4: A549 cell lysate<br />Lane 5: K-562 cell lysate<br />Lane 6: COS-1 cell lysate<br />Lane 7: NIH/3T3 cell lysate<br />Lane 8: C2C12 cell lysate<br />Lane 9: PC-12 cell lysate<br /><br />Lysates/proteins at 30 µg/Lane.<br /><br />Predicted band size: 70 kDa<br />Observed band size: 70/75 kDa<br /><br />Exposure time: 3 minutes 10 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/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a>) at 1/1,000 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 FXR1 on different lysates with Rabbit anti-FXR1 antibody (HA721669) at 1/1,000 dilution.

    Lane 1: HeLa cell lysate
    Lane 2: 293T cell lysate
    Lane 3: HepG2 cell lysate
    Lane 4: A549 cell lysate
    Lane 5: K-562 cell lysate
    Lane 6: COS-1 cell lysate
    Lane 7: NIH/3T3 cell lysate
    Lane 8: C2C12 cell lysate
    Lane 9: PC-12 cell lysate

    Lysates/proteins at 30 µg/Lane.

    Predicted band size: 70 kDa
    Observed band size: 70/75 kDa

    Exposure time: 3 minutes 10 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 (HA721669) at 1/1,000 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.

  • Immunohistochemical analysis of paraffin-embedded human testis tissue with Rabbit anti-FXR1 antibody (<a href="/products/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a>) at 1/200 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/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a>) at 1/200 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 human testis tissue with Rabbit anti-FXR1 antibody (HA721669) at 1/200 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 (HA721669) at 1/200 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 with Rabbit anti-FXR1 antibody (<a href="/products/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a>) at 1/200 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/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a>) at 1/200 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 with Rabbit anti-FXR1 antibody (HA721669) at 1/200 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 (HA721669) at 1/200 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 rat brain tissue with Rabbit anti-FXR1 antibody (<a href="/products/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a>) at 1/200 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/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a>) at 1/200 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 rat brain tissue with Rabbit anti-FXR1 antibody (HA721669) at 1/200 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 (HA721669) at 1/200 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.

  • Immunocytochemistry analysis of PC-12 cells labeling FXR1 with Rabbit anti-FXR1 antibody (<a href="/products/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a>) at 1/100 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-FXR1 antibody (<a href="/products/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a>) at 1/100 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.

    Immunocytochemistry analysis of PC-12 cells labeling FXR1 with Rabbit anti-FXR1 antibody (HA721669) at 1/100 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-FXR1 antibody (HA721669) at 1/100 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.

  • FXR1 was immunoprecipitated from 0.2 mg HepG2 cell lysate with <a href="/products/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a> at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using <a href="/products/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a> at 1/1,000 dilution. HRP Conjugated Anti-Rabbit IgG for IP Nano-secondary antibody at 1/5,000 dilution was used for 1 hour at room temperature.<br /><br />Lane 1: HepG2 cell lysate (input)<br />Lane 2: <a href="/products/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a> IP in HepG2 cell lysate<br />Lane 3: Rabbit IgG instead of <a href="/products/HA721669" style="font-weight: bold;text-decoration: underline;">HA721669</a> in HepG2 cell lysate<br /><br />Blocking/Dilution buffer: primary antibody dilution (K1803)<br />Exposure time: 10 seconds; ECL: K1801

    FXR1 was immunoprecipitated from 0.2 mg HepG2 cell lysate with HA721669 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using HA721669 at 1/1,000 dilution. HRP Conjugated Anti-Rabbit IgG for IP Nano-secondary antibody at 1/5,000 dilution was used for 1 hour at room temperature.

    Lane 1: HepG2 cell lysate (input)
    Lane 2: HA721669 IP in HepG2 cell lysate
    Lane 3: Rabbit IgG instead of HA721669 in HepG2 cell lysate

    Blocking/Dilution buffer: primary antibody dilution (K1803)
    Exposure time: 10 seconds; ECL: K1801

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