Skip to content

INPP4A Recombinant Rabbit Monoclonal Antibody [PSH01-27]

Usd: 385

Specification

Bulk Order Quote | Customization Request

Catalog# HA721651

INPP4A Recombinant Rabbit Monoclonal Antibody [PSH01-27]

Application

  • WB

  • IHC-P

  • IF-Cell

Reactivity

  • Human

  • Mouse

  • Rat

BSA and Azide free
Conjugation

  • unconjugated

Overview

Product Name

INPP4A Recombinant Rabbit Monoclonal Antibody [PSH01-27]

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Recombinant protein within human INPP4A aa 1-250 / 977.

Species Reactivity

Human, Mouse, Rat

Validated Applications

WB, IHC-P, IF-Cell

Target Molecular Weight

Predicted band size: 110 kDa

Positive Control

Jurkat cell lysate, 293T cell lysate, mouse brain tissue lysate, rat brain tissue lysate, Jurkat, rat brain tissue, mouse brain tissue.

Conjugation

unconjugated

Clone Number

PSH01-27

RRID

AB_3072764

Reactivity Data

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

Product Features

Form

Liquid

Concentration

1 mg/mL.(The concentration of this product may be batch-dependent)

Storage Instructions

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

Storage Buffer

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

Isotype

IgG

Purification Method

Protein A affinity purified.

Application Dilution

  • WB

  • 1:1,000-1:5,000

  • IHC-P

  • 1:200

  • IF-Cell

  • 1:100

Target

Function

Type I inositol-3,4-bisphosphate 4-phosphatase is an enzyme that in humans is encoded by the INPP4A gene. INPP4A encodes the inositol polyphosphate 4-phosphatase type I, one of the enzymes involved in phosphatidylinositol signaling pathways. This enzyme removes the phosphate group at position 4 of the inositol ring from inositol 3,4-bisphosphate.

Background References

1. Tan H et al. The hMeDIP-Seq identified INPP4A as a novel biomarker for eosinophilic chronic rhinosinusitis with nasal polyps. Epigenomics. 2022 Jun

2. Zhou Y et al. MicroRNA-223-3p regulates allergic inflammation by targeting INPP4A. Braz J Otorhinolaryngol. 2021 Sep-Oct

Subcellular Location

Early endosome membrane, Recycling endosome membrane, Cell membrane, Nucleus, Cytoplasm, Postsynaptic density.

UNIPROT

SwissProt: Q96PE3 Human

SwissProt: Q9EPW0 Mouse

SwissProt: Q62784 Rat

Synonyms

107kDa antibody

4-bisphosphate 4-phosphatase antibody

9630012D15 antibody

D130048C09Rik antibody

Inositol polyphosphate 4 phosphatase type I 107kDa antibody

Inositol polyphosphate 4 phosphatase type I antibody

Inositol polyphosphate 4-phosphatase type I antibody

INP4A_HUMAN antibody

INPP4 antibody

Inpp4a antibody

Expand

Images

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />Western blot analysis of INPP4A on different lysates with Rabbit anti-INPP4A antibody (<a href="/products/HA721651" style="font-weight: bold;text-decoration: underline;">HA721651</a>) at 1/5,000 dilution and competitor's antibody at 1/1,000 dilution.<br /><br />Lane 1: Jurkat cell lysate<br />Lane 2: 293T cell lysate<br />Lane 3: Mouse brain tissue lysate<br />Lane 4: Mouse liver tissue lysate (low expression)<br />Lane 5: Rat brain tissue lysate<br />Lane 6: Rat liver tissue lysate (low expression)<br /><br />Lysates/proteins at 20 µg/Lane.<br /><br />Predicted band size: 110 kDa<br />Observed band size: 110 kDa<br /><br />Exposure time: 1 minute; ECL: K1802;<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/HA721651" style="font-weight: bold;text-decoration: underline;">HA721651</a>) at 1/5,000 dilution and competitor's antibody at 1/1,000 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.

    ☑ Relative expression (RE)

    Western blot analysis of INPP4A on different lysates with Rabbit anti-INPP4A antibody (HA721651) at 1/5,000 dilution and competitor's antibody at 1/1,000 dilution.

    Lane 1: Jurkat cell lysate
    Lane 2: 293T cell lysate
    Lane 3: Mouse brain tissue lysate
    Lane 4: Mouse liver tissue lysate (low expression)
    Lane 5: Rat brain tissue lysate
    Lane 6: Rat liver tissue lysate (low expression)

    Lysates/proteins at 20 µg/Lane.

    Predicted band size: 110 kDa
    Observed band size: 110 kDa

    Exposure time: 1 minute; ECL: K1802;

    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 (HA721651) at 1/5,000 dilution and competitor's antibody at 1/1,000 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.

  • Immunocytochemistry analysis of Jurkat cells labeling INPP4A with Rabbit anti-INPP4A antibody (<a href="/products/HA721651" style="font-weight: bold;text-decoration: underline;">HA721651</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-INPP4A antibody (<a href="/products/HA721651" style="font-weight: bold;text-decoration: underline;">HA721651</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 Jurkat cells labeling INPP4A with Rabbit anti-INPP4A antibody (HA721651) 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-INPP4A antibody (HA721651) 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.

  • Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rabbit anti-INPP4A antibody (<a href="/products/HA721651" style="font-weight: bold;text-decoration: underline;">HA721651</a>) at 1/200 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 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/HA721651" style="font-weight: bold;text-decoration: underline;">HA721651</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-INPP4A antibody (HA721651) at 1/200 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 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 (HA721651) 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-INPP4A antibody (<a href="/products/HA721651" style="font-weight: bold;text-decoration: underline;">HA721651</a>) at 1/200 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 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/HA721651" style="font-weight: bold;text-decoration: underline;">HA721651</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-INPP4A antibody (HA721651) at 1/200 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 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 (HA721651) 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.

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />Immunohistochemical analysis of paraffin-embedded mouse liver tissue (low expression) with Rabbit anti-INPP4A antibody (<a href="/products/HA721651" style="font-weight: bold;text-decoration: underline;">HA721651</a>) at 1/200 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 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/HA721651" style="font-weight: bold;text-decoration: underline;">HA721651</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.

    ☑ Relative expression (RE)

    Immunohistochemical analysis of paraffin-embedded mouse liver tissue (low expression) with Rabbit anti-INPP4A antibody (HA721651) at 1/200 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 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 (HA721651) 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.

  • <span style="font-weight: bold;">☑ Knockdown (KD)</span><br /><br />Western blot analysis of INPP4A on different lysates with Rabbit anti-INPP4A antibody (<a href="/products/HA721651" style="font-weight: bold;text-decoration: underline;">HA721651</a>) at 1/2,000 dilution.<br /><br />Lane 1: 293T-si NT cell lysate<br />Lane 2: 293T-si INPP4A cell lysate<br /><br />Lysates/proteins at 10 µg/Lane.<br /><br />Predicted band size: 110 kDa<br />Observed band size: 110 kDa<br /><br />Exposure time: 1 minute 58 seconds; 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/HA721651" style="font-weight: bold;text-decoration: underline;">HA721651</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 1/100,000 dilution was used for 1 hour at room temperature.

    ☑ Knockdown (KD)

    Western blot analysis of INPP4A on different lysates with Rabbit anti-INPP4A antibody (HA721651) at 1/2,000 dilution.

    Lane 1: 293T-si NT cell lysate
    Lane 2: 293T-si INPP4A cell lysate

    Lysates/proteins at 10 µg/Lane.

    Predicted band size: 110 kDa
    Observed band size: 110 kDa

    Exposure time: 1 minute 58 seconds; 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 (HA721651) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/100,000 dilution was used for 1 hour at room temperature.

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