Skip to content

NAPSIN A Recombinant Mouse Monoclonal Antibody [A9C1-R] - BSA and Azide free

Usd: 649

Specification

Bulk Order Quote | Customization Request

Catalog# HA610175

NAPSIN A Recombinant Mouse Monoclonal Antibody [A9C1-R] - BSA and Azide free

Application

  • IHC-P

Reactivity

  • Human

With BSA and Azide
Conjugation

  • unconjugated

Overview

Product Name

NAPSIN A Recombinant Mouse Monoclonal Antibody [A9C1-R] - BSA and Azide free

Antibody Type

Recombinant Mouse Monoclonal Antibody

Immunogen

Recombinant protein within human NAPSIN A aa 51-200 / 420.

Species Reactivity

Human

Validated Applications

IHC-P

Target Molecular Weight

Predicted band size: 45 kDa

Positive Control

Human kidney tissue, human lung cancer tissue.

Conjugation

unconjugated

Clone Number

A9C1-R

Product Features

Form

Liquid

Concentration

1mg/ml

Storage Instructions

Store at 2-8℃. Avoid freeze.

Storage Buffer

1*PBS (pH7.4).

Isotype

IgG1

Purification Method

Protein A affinity purified.

Application Dilution

Target

Function

Napsin-A is an aspartic proteinase that is encoded in humans by the NAPSA gene. The name napsin comes from novel aspartic proteinase of the pepsin family. The activation peptide of an aspartic proteinase acts as an inhibitor of the active site. These peptide segments, or pro-parts, are deemed important for correct folding, targeting, and control of the activation of aspartic proteinase zymogens. The pronapsin A gene is expressed predominantly in lung and kidney. Its translation product is predicted to be a fully functional, glycosylated aspartic proteinase precursor containing an RGD motif and an additional 18 residues at its C-terminus. Detection of NAPSA gene expression can be used to distinguish adenocarcinomas from other forms of lung cancer.

Background References

1. Weidemann S et al. Napsin A Expression in Human Tumors and Normal Tissues. Pathol Oncol Res. 2021 Apr

2. Wu J et al. Napsin A Expression in Subtypes of Thyroid Tumors: Comparison with Lung Adenocarcinomas. Endocr Pathol. 2020 Mar

Subcellular Location

Secreted.

UNIPROT

SwissProt: O96009 Human

Synonyms

Asp 4 antibody

ASP4 antibody

Aspartyl protease 4 antibody

KAP antibody

Kdap antibody

Kidney derived aspartic protease like protein antibody

NAP1 antibody

NAPA antibody

Napsa antibody

NAPSA_HUMAN antibody

Expand

Images

  • This data was developed using <a href="/products/HA601302" style="font-weight: bold;text-decoration: underline;">HA601302</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded human kidney tissue with Mouse anti-NAPSIN A antibody (<a href="/products/HA601302" style="font-weight: bold;text-decoration: underline;">HA601302</a>) at 1/2,000 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/HA601302" style="font-weight: bold;text-decoration: underline;">HA601302</a>) at 1/2,000 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.

    This data was developed using HA601302, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded human kidney tissue with Mouse anti-NAPSIN A antibody (HA601302) at 1/2,000 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 (HA601302) at 1/2,000 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.

  • This data was developed using <a href="/products/HA601302" style="font-weight: bold;text-decoration: underline;">HA601302</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded human lung cancer tissue with Mouse anti-NAPSIN A antibody (<a href="/products/HA601302" style="font-weight: bold;text-decoration: underline;">HA601302</a>) at 1/2,000 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/HA601302" style="font-weight: bold;text-decoration: underline;">HA601302</a>) at 1/2,000 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.

    This data was developed using HA601302, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded human lung cancer tissue with Mouse anti-NAPSIN A antibody (HA601302) at 1/2,000 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 (HA601302) at 1/2,000 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.

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />This data was developed using <a href="/products/HA601302" style="font-weight: bold;text-decoration: underline;">HA601302</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded human colon tissue (negative) with Mouse anti-NAPSIN A antibody (<a href="/products/HA601302" style="font-weight: bold;text-decoration: underline;">HA601302</a>) at 1/2,000 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/HA601302" style="font-weight: bold;text-decoration: underline;">HA601302</a>) at 1/2,000 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.

    ☑ Relative expression (RE)

    This data was developed using HA601302, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded human colon tissue (negative) with Mouse anti-NAPSIN A antibody (HA601302) at 1/2,000 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 (HA601302) at 1/2,000 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"