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IP3 receptor Recombinant Mouse Monoclonal Antibody [PSH14-18] - BSA and Azide free

Usd: 649

Specification

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Catalog# HA610290

IP3 receptor Recombinant Mouse Monoclonal Antibody [PSH14-18] - BSA and Azide free

Application

  • WB

  • IHC-P

Reactivity

  • Mouse

  • Rat

With BSA and Azide
Conjugation

  • unconjugated

Overview

Product Name

IP3 receptor Recombinant Mouse Monoclonal Antibody [PSH14-18] - BSA and Azide free

Antibody Type

Recombinant Mouse Monoclonal Antibody

Immunogen

Recombinant protein within Rat IP3 receptor aa 2591-2750 (Cytoplasmic).

Species Reactivity

Mouse, Rat

Validated Applications

WB, IHC-P

Molecular Weight

Predicted band size: 313 kDa

Positive Control

Mouse brain tissue lysate, mouse brain tissue, rat brain tissue.

Conjugation

unconjugated

Clone Number

PSH14-18

Product Features

Form

Liquid

Concentration

1mg/ml

Storage Instructions

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

Storage Buffer

1*PBS (pH7.4).

Isotype

IgG1

Purification Method

Protein A affinity purified.

Application Dilution

  • WB

  • 1:5,000

  • IHC-P

  • 1:1,000

Target

Function

Inositol 1,4,5-trisphosphate-gated calcium channel that, upon inositol 1,4,5-trisphosphate binding, mediates calcium release from the endoplasmic reticulum (ER) and participates in calcium oscillations. Undergoes conformational changes upon ligand binding, suggesting structural flexibility that allows the channel to switch from a closed state, capable of interacting with its ligands such as inositol 1,4,5-trisphosphate and Ca2+, to an open state, capable of transferring calcium ions across the ER membrane (By similarity). Cytoplasmic calcium, released from the ER, triggers apoptosis by the activation of CAMK2 complex. Part of a complex composed of HSPA9, ITPR1 and VDAC1 that regulates mitochondrial calcium-dependent apoptosis by facilitating calcium transport from the ER lumen to the mitochondria intermembrane space thus providing calcium for the downstream calcium channel MCU that directly releases it into mitochondria matrix. Involved in the regulation of epithelial secretion of electrolytes and fluid through the interaction with AHCYL1. Regulates fertilization and egg activation by tuning the frequency and amplitude of calcium oscillations.

Background References

1. Wu L et al. Type 3 IP3 receptor: Its structure, functions, and related disease implications. Channels (Austin). 2023 Dec

2. Dridi H et al. IP3 receptor orchestrates maladaptive vascular responses in heart failure. J Clin Invest. 2022 Feb

Subcellular Location

Endoplasmic reticulum membrane, Cytoplasmic vesicle, secretory vesicle membrane, Cytoplasm, perinuclear region.

UNIPROT

SwissProt: P11881 Mouse

SwissProt: P29994 Rat

Synonyms

4 antibody

5-trisphosphate receptor antibody

5-trisphosphate receptor type 1 antibody

DKFZp313E1334 antibody

DKFZp313N1434 antibody

inositol 1 4 5 triphosphate receptor type 1 antibody

Inositol 1 4 5 trisphosphate Receptor Type 1 antibody

Inositol 1 antibody

InsP3R1 antibody

IP3 antibody

Expand

Images

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />Western blot analysis of IP3 receptor on different lysates with Mouse anti-IP3 receptor antibody (<a href="/products/HA610290" style="font-weight: bold;text-decoration: underline;">HA610290</a>) at 1/5,000 dilution.<br /><br />Lane 1: Mouse skeletal muscle tissue lysate (negative) (40 µg/Lane)<br />Lane 2: Mouse brain tissue lysate (40 µg/Lane)<br /><br />Predicted band size: 313 kDa<br />Observed band size: 313 kDa<br /><br />Exposure time: 59 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/HA610290" style="font-weight: bold;text-decoration: underline;">HA610290</a>) at 1/5,000 dilution was used in primary antibody dilution (<a href="/products/K1803" style="font-weight: bold;text-decoration: underline;">K1803</a>) 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.

    ☑ Relative expression (RE)

    Western blot analysis of IP3 receptor on different lysates with Mouse anti-IP3 receptor antibody (HA610290) at 1/5,000 dilution.

    Lane 1: Mouse skeletal muscle tissue lysate (negative) (40 µg/Lane)
    Lane 2: Mouse brain tissue lysate (40 µg/Lane)

    Predicted band size: 313 kDa
    Observed band size: 313 kDa

    Exposure time: 59 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 (HA610290) at 1/5,000 dilution was used in primary antibody dilution (K1803) at 4℃ overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1/50,000 dilution was used for 1 hour at room temperature.

  • Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Mouse anti-IP3 receptor antibody (<a href="/products/HA610290" style="font-weight: bold;text-decoration: underline;">HA610290</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/HA610290" style="font-weight: bold;text-decoration: underline;">HA610290</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 brain tissue with Mouse anti-IP3 receptor antibody (HA610290) 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 (HA610290) 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 rat brain tissue with Mouse anti-IP3 receptor antibody (<a href="/products/HA610290" style="font-weight: bold;text-decoration: underline;">HA610290</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/HA610290" style="font-weight: bold;text-decoration: underline;">HA610290</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 rat brain tissue with Mouse anti-IP3 receptor antibody (HA610290) 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 (HA610290) 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.

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