Skip to content

GPX4 Recombinant Rabbit Monoclonal Antibody [JU11-31]

見積もりを依頼する

お問い合わせ

E-mail: [email protected]

TEL: 0571-88062880

代理店・販売店を探す

Catalog# ET1706-45

GPX4 Recombinant Rabbit Monoclonal Antibody [JU11-31]

Application

  • WB

  • IHC-P

  • IF-Cell

  • FC

Reactivity

  • Human

  • Mouse

  • Rat

  • Zebrafish

BSA and Azide free
Predicted reactivity

  • Pig

  • Cynomolgus monkey

予測される交差反応性
Conjugation

  • unconjugated

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

製品概要

製品名

GPX4 Recombinant Rabbit Monoclonal Antibody [JU11-31]

抗体のタイプ

Recombinant Rabbit monoclonal Antibody

免疫原

Synthetic peptide within Human GPX4 aa 23-72 / 197.

交差反応性（対応種属）

Human, Mouse, Rat, Zebrafish (Predicted: Pig, Cynomolgus monkey)

予測される交差反応性

検証済みアプリケーション

WB, IHC-P, IF-Cell, FC

分子量

Predicted band size: 22 kDa

ポジティブコントロール

HeLa cell lysate, A549 cell lysate, HepG2 cell lysate, U-937 cell lysate, HEK-293 cell lysate, Mouse testis tissue lysate, Rat testis tissue lysate, Mouse kidney tissue lysate, Rat kidney tissue lysate, Mouse brain tissue lysate, Rat brain tissue lysate, zebrafish tissue lysates, NIH/3T3 cell lysate, Neuro-2a cell lysate, RAW264.7 cell lysate, M-NFS-60 cell lysate, C6 cell lysate, PC-12 cell lysate, HEK-293, human kidney tissue, mouse kidney tissue, mouse testis tissue, C6.

コンジュゲーション

unconjugated

クローン番号

JU11-31

RRID

AB_3070665

製品の特徴

形態

Liquid

濃度

保存方法

Shipped at 4℃. Store at +4℃ short term (1-2 weeks). Store at -20℃ long term.

保存バッファー

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

アイソタイプ

IgG

精製方法

Protein A affinity purified.

推奨希釈倍率

  • WB

  • 1:5,000-1:10,000

  • IHC-P

  • 1:1,000-1:5,000

  • IF-Cell

  • 1:50-1:200

  • FC

  • 1:1,000

ターゲット

機能

Glutathione peroxidase (GPx) enzymes are generally selenium-containing tetrameric glycoproteins that help prevent lipid peroxidation of cell membranes. GPx enzymes reduce lipid hydroperoxides to alcohols, and reduce free hydrogen peroxide to water. GPx members are among the few proteins known in higher vertebrates to contain selenocysteine, which occurs at the active site of glutathione peroxidase and is coded by the nonsense (stop) codon TGA. There are eight GPx homologs (GPx-1-8). GPx-1, Gpx-2 and Gpx-3 exist as homotetramers. Gpx-4 has a high tendancy to form high molecular weight oligomers.

背景・参考文献

1. Luna-Sánchez M et al. CoQ deficiency causes disruption of mitochondrial sulfide oxidation, a new pathomechanism associated with this syndrome. EMBO Mol Med 9:78-95 (2017).

2. Kagan VE et al. Oxidized arachidonic and adrenic PEs navigate cells to ferroptosis. Nat Chem Biol 13:81-90 (2017).

配列相同性

Belongs to the glutathione peroxidase family.

組織特異性

Present primarily in testis. Expressed in platelets (at protein level).

サブセルラー局在

Mitochondrion, Cytoplasm.

UNIPROT #

SwissProt: P36969 Human

SwissProt: O70325 Mouse

SwissProt: P36970 Rat

別名

Glutathione peroxidase 4 antibody

GPX 4 antibody

GPX-4 antibody

GPX4 antibody

GPX4_HUMAN antibody

GSHPx-4 antibody

MCSP antibody

mitochondrial antibody

PHGPx antibody

Phospholipid hydroperoxidase antibody

詳細を見る

画像

  • Western blot analysis of GPX4 on different lysates with Rabbit anti-GPX4 antibody (<a href="/products/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</a>) at 1/10,000 dilution and competitor's antibody at 1/10,000 dilution.<br /><br />Lane 1: HeLa cell lysate (20 µg/Lane)<br />Lane 2: A549 cell lysate (20 µg/Lane)<br />Lane 3: HepG2 cell lysate (20 µg/Lane)<br />Lane 4: U-937 cell lysate (20 µg/Lane)<br />Lane 5: HEK-293 cell lysate (20 µg/Lane)<br />Lane 6: Mouse testis tissue lysate (20 µg/Lane)<br />Lane 7: Rat testis tissue lysate (20 µg/Lane)<br />Lane 8: Mouse kidney tissue lysate (20 µg/Lane)<br />Lane 9: Rat kidney tissue lysate (20 µg/Lane)<br />Lane 10: Mouse brain tissue lysate (20 µg/Lane)<br />Lane 11: Rat brain tissue lysate (20 µg/Lane)<br /><br />Predicted band size: 22 kDa<br />Observed band size: 20 kDa<br />Exposure time: 2 minutes; ECL: K1801;<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/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</a>) at 1/10,000 dilution and competitor's antibody at 1/10,000 dilution were 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.

    Western blot analysis of GPX4 on different lysates with Rabbit anti-GPX4 antibody (ET1706-45) at 1/10,000 dilution and competitor's antibody at 1/10,000 dilution.

    Lane 1: HeLa cell lysate (20 µg/Lane)
    Lane 2: A549 cell lysate (20 µg/Lane)
    Lane 3: HepG2 cell lysate (20 µg/Lane)
    Lane 4: U-937 cell lysate (20 µg/Lane)
    Lane 5: HEK-293 cell lysate (20 µg/Lane)
    Lane 6: Mouse testis tissue lysate (20 µg/Lane)
    Lane 7: Rat testis tissue lysate (20 µg/Lane)
    Lane 8: Mouse kidney tissue lysate (20 µg/Lane)
    Lane 9: Rat kidney tissue lysate (20 µg/Lane)
    Lane 10: Mouse brain tissue lysate (20 µg/Lane)
    Lane 11: Rat brain tissue lysate (20 µg/Lane)

    Predicted band size: 22 kDa
    Observed band size: 20 kDa
    Exposure time: 2 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 (ET1706-45) at 1/10,000 dilution and competitor's antibody at 1/10,000 dilution were 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.

  • <span style="font-weight: bold;">☑ Knockdown (KD)</span><br /><br />Western blot analysis of GPX4 on different lysates with Rabbit anti-GPX4 antibody (<a href="/products/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</a>) at 1/10,000 dilution.<br /><br />Lane 1: Hela-si NT cell lysate, 10 µg/Lane<br />Lane 2: Hela-si GPX4 cell lysate, 10 µg/Lane<br /><br />Predicted band size: 22 kDa<br />Observed band size: 20,22 kDa<br />Exposure time: 1 minutes 40 seconds;<br />4-20% SDS-PAGE gel.<br /><br /><a href="/products/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</a> was shown to specifically react with GPX4 in Hela-si NT cells. Weakened band was observed when Hela-si GPX4 sample was tested. Hela-si NT and Hela-si GPX4 samples were subjected to SDS-PAGE. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM in TBST for 1 hour at room temperature. The primary antibody (<a href="/products/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</a>, 1/10,000) and Loading control antibody (Rabbit anti-GAPDH , <a href="/products/ET1601-4" style="font-weight: bold;text-decoration: underline;">ET1601-4</a>, 1/10,000) were used in 5% BSA 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 1:300,000 dilution was used for 1 hour at room temperature.

    ☑ Knockdown (KD)

    Western blot analysis of GPX4 on different lysates with Rabbit anti-GPX4 antibody (ET1706-45) at 1/10,000 dilution.

    Lane 1: Hela-si NT cell lysate, 10 µg/Lane
    Lane 2: Hela-si GPX4 cell lysate, 10 µg/Lane

    Predicted band size: 22 kDa
    Observed band size: 20,22 kDa
    Exposure time: 1 minutes 40 seconds;
    4-20% SDS-PAGE gel.

    ET1706-45 was shown to specifically react with GPX4 in Hela-si NT cells. Weakened band was observed when Hela-si GPX4 sample was tested. Hela-si NT and Hela-si GPX4 samples were subjected to SDS-PAGE. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM in TBST for 1 hour at room temperature. The primary antibody (ET1706-45, 1/10,000) and Loading control antibody (Rabbit anti-GAPDH , ET1601-4, 1/10,000) were used in 5% BSA at room temperature for 2 hours. Goat Anti-rabbit IgG-HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature.

  • Immunocytochemistry analysis of HEK-293 cells labeling GPX4 with Rabbit anti-GPX4 antibody (<a href="/products/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</a>) at 1/200 dilution and competitor's antibody 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-GPX4 antibody (<a href="/products/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</a>) at 1/200 dilution and competitor's antibody 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.

    Immunocytochemistry analysis of HEK-293 cells labeling GPX4 with Rabbit anti-GPX4 antibody (ET1706-45) at 1/200 dilution and competitor's antibody 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-GPX4 antibody (ET1706-45) at 1/200 dilution and competitor's antibody 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.

  • Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-GPX4 antibody (<a href="/products/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</a>) at 1/1,000 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/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</a>) at 1/1,000 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 human kidney tissue with Rabbit anti-GPX4 antibody (ET1706-45) at 1/1,000 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 (ET1706-45) at 1/1,000 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 kidney tissue with Rabbit anti-GPX4 antibody (<a href="/products/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</a>) at 1/1,000 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/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</a>) at 1/1,000 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 kidney tissue with Rabbit anti-GPX4 antibody (ET1706-45) at 1/1,000 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 (ET1706-45) at 1/1,000 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 testis tissue with Rabbit anti-GPX4 antibody (<a href="/products/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</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/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</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 testis tissue with Rabbit anti-GPX4 antibody (ET1706-45) 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 (ET1706-45) 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.

  • Immunocytochemistry analysis of C6 cells labeling GPX4 with Rabbit anti-GPX4 antibody (<a href="/products/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</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-GPX4 antibody (<a href="/products/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</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 C6 cells labeling GPX4 with Rabbit anti-GPX4 antibody (ET1706-45) 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-GPX4 antibody (ET1706-45) 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.

  • Flow cytometric analysis of HEK-293 cells labeling GPX4.<br /><br />Cells were fixed and permeabilized. Then stained with the primary antibody (<a href="/products/ET1706-45" style="font-weight: bold;text-decoration: underline;">ET1706-45</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).

    Flow cytometric analysis of HEK-293 cells labeling GPX4.

    Cells were fixed and permeabilized. Then stained with the primary antibody (ET1706-45, 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).

ご注意: 本製品はすべて「研究用試薬」です。人や動物の診断・治療目的、または臨床診断には使用できません。（FOR RESEARCH USE ONLY）

文献・引用論文

同一ターゲット＆同一シグナル伝達経路の関連製品

metafield image

GPX4 Rabbit Polyclonal Antibody

Application: WB

Reactivity: Mouse,Rat

Conjugate: unconjugated

metafield image

GPX4 Recombinant Rabbit Monoclonal Antibody [JU11-31] - BSA and Azide free

Application: WB,IHC-P,IF-Cell,FC

Reactivity: Human,Mouse,Rat,Zebrafish,Pig,Cynomolgus monkey

Conjugate: unconjugated

Close (esc)

Popup

Use this popup to embed a mailing list sign up form. Alternatively use it as a simple call to action with a link to a product or a page.

Age verification

By clicking enter you are verifying that you are old enough to consume alcohol.

Enter

搜索

主菜单