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Steroid sulfatase Recombinant Rabbit Monoclonal Antibody [PSH05-74] - BSA and Azide free

Usd: 649

Specification

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Catalog# HA751024

Steroid sulfatase Recombinant Rabbit Monoclonal Antibody [PSH05-74] - BSA and Azide free

Application

  • WB

  • IHC-P

Reactivity

  • Human

With BSA and Azide
Conjugation

  • unconjugated

Overview

Product Name

Steroid sulfatase Recombinant Rabbit Monoclonal Antibody [PSH05-74] - BSA and Azide free

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Recombinant protein within Human Steroid sulfatase aa 22-184 and aa 235-583.

Species Reactivity

Human

Validated Applications

WB, IHC-P

Target Molecular Weight

Predicted band size: 65 kDa

Positive Control

Jurkat cell lysate HepG2 cell lysate, MCF7 cell lysate, Huh7 cell lysate, T-47D cell lysate, human placenta tissue.

Conjugation

unconjugated

Clone Number

PSH05-74

Product Features

Form

Liquid

Concentration

1mg/ml

Storage Instructions

Store at 2-8℃. Avoid freeze.

Storage Buffer

1*PBS (pH7.4).

Isotype

IgG

Purification Method

Protein A affinity purified.

Application Dilution

Target

Function

Catalyzes the conversion of sulfated steroid precursors, such as dehydroepiandrosterone sulfate (DHEA-S) and estrone sulfate to the free steroid. Defects in STS are the cause of ichthyosis X-linked (IXL) [MIM:308100]. Ichthyosis X-linked is a keratinization disorder manifesting with mild erythroderma and generalized exfoliation of the skin within a few weeks after birth. Affected boys later develop large, polygonal, dark brown scales, especially on the neck, extremities, trunk, and buttocks.

Background References

1. Oyama N., Satoh M., Iwatsuki K., Kaneko F. Novel point mutations in the steroid sulfatase gene in patients with X- linked ichthyosis: transfection analysis using the mutated genes. J. Invest. Dermatol. 114:1195-1199 (2000)

2. Matsumoto J., Ariyoshi N., Ishii I., Kitada M. Functional characterization of seven single-nucleotide polymorphisms of the steroid sulfatase gene found in a Japanese population. J. Hum. Genet. 58:267-272 (2013)

Subcellular Location

Cytoplasmic vesicle. Endoplasmic reticulum.

UNIPROT

SwissProt: P08842 Human

Synonyms

ARSC antibody

ARSC1 antibody

Arylsulfatase C antibody

Arylsulfatase C isozyme S antibody

ASC antibody

EC 3.1.6.2 antibody

ES antibody

Estrone sulfatase antibody

SSDD antibody

Steroid sulfatase (microsomal) antibody

Expand

Images

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />This data was developed using <a href="/products/HA722441" style="font-weight: bold;text-decoration: underline;">HA722441</a>, the same antibody clone in a different buffer formulation.<br />Western blot analysis of Steroid sulfatase on different lysates with Rabbit anti-Steroid sulfatase antibody (<a href="/products/HA722441" style="font-weight: bold;text-decoration: underline;">HA722441</a>) at 1/2,000 dilution and competitor's antibody at 1/2,000 dilution.<br /><br />Lane 1: Jurkat cell lysate<br />Lane 2: LNCaP cell lysate (negative)<br />Lane 3: HepG2 cell lysate<br />Lane 4: MCF7 cell lysate<br />Lane 5: Huh7 cell lysate<br />Lane 6: T-47D cell lysate<br /><br />Lysates/proteins at 20 µg/Lane.<br /><br />Predicted band size: 65 kDa<br />Observed band size: 65 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/HA722441" style="font-weight: bold;text-decoration: underline;">HA722441</a>) at 1/2,000 dilution and competitor's antibody at 1/2,000 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)

    This data was developed using HA722441, the same antibody clone in a different buffer formulation.
    Western blot analysis of Steroid sulfatase on different lysates with Rabbit anti-Steroid sulfatase antibody (HA722441) at 1/2,000 dilution and competitor's antibody at 1/2,000 dilution.

    Lane 1: Jurkat cell lysate
    Lane 2: LNCaP cell lysate (negative)
    Lane 3: HepG2 cell lysate
    Lane 4: MCF7 cell lysate
    Lane 5: Huh7 cell lysate
    Lane 6: T-47D cell lysate

    Lysates/proteins at 20 µg/Lane.

    Predicted band size: 65 kDa
    Observed band size: 65 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 (HA722441) at 1/2,000 dilution and competitor's antibody at 1/2,000 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.

  • This data was developed using <a href="/products/HA722441" style="font-weight: bold;text-decoration: underline;">HA722441</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded human placenta tissue with Rabbit anti-Steroid sulfatase antibody (<a href="/products/HA722441" style="font-weight: bold;text-decoration: underline;">HA722441</a>) at 1/3,000 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/HA722441" style="font-weight: bold;text-decoration: underline;">HA722441</a>) at 1/3,000 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 HA722441, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded human placenta tissue with Rabbit anti-Steroid sulfatase antibody (HA722441) at 1/3,000 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 (HA722441) at 1/3,000 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/HA722441" style="font-weight: bold;text-decoration: underline;">HA722441</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded human pancreas tissue (negative) with Rabbit anti-Steroid sulfatase antibody (<a href="/products/HA722441" style="font-weight: bold;text-decoration: underline;">HA722441</a>) at 1/3,000 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/HA722441" style="font-weight: bold;text-decoration: underline;">HA722441</a>) at 1/3,000 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 HA722441, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded human pancreas tissue (negative) with Rabbit anti-Steroid sulfatase antibody (HA722441) at 1/3,000 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 (HA722441) at 1/3,000 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"