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SCD1 Recombinant Rabbit Monoclonal Antibody [PSH15-47] - BSA and Azide free

Usd: 649

Specification

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Catalog# HA751562

SCD1 Recombinant Rabbit Monoclonal Antibody [PSH15-47] - BSA and Azide free

Application

  • WB

  • IHC-Fr

  • IHC-P

  • FC

Reactivity

  • Mouse

  • Rat

With BSA and Azide
Conjugation

  • unconjugated

Overview

Product Name

SCD1 Recombinant Rabbit Monoclonal Antibody [PSH15-47] - BSA and Azide free

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Synthetic peptide within mouse SCD1 aa 1-50.

Species Reactivity

Mouse, Rat

Validated Applications

WB, IHC-Fr, IHC-P, FC

Target Molecular Weight

Predicted band size: 41 kDa

Positive Control

Mouse liver tissue lysate, Mouse white adipose tissue lysate, Mouse brown adipose tissue lysate, Rat white adipose tissue lysate, mouse adipose tissue, mouse liver tissue, rat adipose tissue, rat liver tissue, MC/9.

Conjugation

unconjugated

Clone Number

PSH15-47

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

Stearoyl-CoA desaturase (Δ-9-desaturase or SCD-1) is an endoplasmic reticulum enzyme that catalyzes the rate-limiting step in the formation of monounsaturated fatty acids (MUFAs), specifically oleate and palmitoleate from stearoyl-CoA and palmitoyl-CoA. Oleate and palmitoleate are major components of membrane phospholipids, cholesterol esters and alkyl-diacylglycerol. In humans, the enzyme is present in two isoforms, encoded respectively by the SCD1 and SCD5 genes. Stearoyl-CoA desaturase-1 is a key enzyme in fatty acid metabolism. It is responsible for forming a double bond in stearoyl-CoA. This is how the monounsaturated fatty acid oleic acid is produced from the saturated fatty acid, stearic acid.

Background References

1. Xuan Y et al. SCD1/FADS2 fatty acid desaturases equipoise lipid metabolic activity and redox-driven ferroptosis in ascites-derived ovarian cancer cells. Theranostics. 2022 Apr

2. Wong TL et al. ADAR1-mediated RNA editing of SCD1 drives drug resistance and self-renewal in gastric cancer. Nat Commun. 2023 May

Subcellular Location

Endoplasmic reticulum membrane, Microsome membrane.

UNIPROT

SwissProt: P13516 Mouse

SwissProt: P07308 Rat

Synonyms

ACOD_HUMAN antibody

Acyl-CoA desaturase antibody

Delta(9)-desaturase antibody

Delta-9 desaturase antibody

Delta-9-Desaturase antibody

FADS5 antibody

Fatty acid desaturase antibody

PRO0998 antibody

SCD 1 antibody

SCD antibody

Expand

Images

  • This data was developed using <a href="/products/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>, the same antibody clone in a different buffer formulation.<br />Western blot analysis of SCD1 on different lysates with Rabbit anti-SCD1 antibody (<a href="/products/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>) at 1/5,000 dilution.<br /><br />Lane 1: Mouse liver tissue lysate<br />Lane 2: Mouse white adipose tissue lysate<br />Lane 3: Mouse brown adipose tissue lysate<br />Lane 4: Rat white adipose tissue lysate<br /><br />Lysates/proteins at 20 µg/Lane.<br /><br />Predicted band size: 41 kDa<br />Observed band size: 37/28 kDa<br /><br />Exposure time: 25 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/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</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-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.

    This data was developed using HA723753, the same antibody clone in a different buffer formulation.
    Western blot analysis of SCD1 on different lysates with Rabbit anti-SCD1 antibody (HA723753) at 1/5,000 dilution.

    Lane 1: Mouse liver tissue lysate
    Lane 2: Mouse white adipose tissue lysate
    Lane 3: Mouse brown adipose tissue lysate
    Lane 4: Rat white adipose tissue lysate

    Lysates/proteins at 20 µg/Lane.

    Predicted band size: 41 kDa
    Observed band size: 37/28 kDa

    Exposure time: 25 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 (HA723753) at 1/5,000 dilution was used in primary antibody dilution (K1803) 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/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>, the same antibody clone in a different buffer formulation.<br />Application: IHC-Fr<br /><br />Species: Mouse<br /><br />Site: liver<br /><br />Sample: Frozen section<br /><br />Antibody concentration: 1/500<br /><br />Antigen retrieval: Not required

    This data was developed using HA723753, the same antibody clone in a different buffer formulation.
    Application: IHC-Fr

    Species: Mouse

    Site: liver

    Sample: Frozen section

    Antibody concentration: 1/500

    Antigen retrieval: Not required

  • This data was developed using <a href="/products/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded mouse adipose tissue with Rabbit anti-SCD1 antibody (<a href="/products/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>) at 1/9,000 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/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>) at 1/9,000 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 HA723753, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded mouse adipose tissue with Rabbit anti-SCD1 antibody (HA723753) at 1/9,000 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 (HA723753) at 1/9,000 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/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded mouse liver tissue with Rabbit anti-SCD1 antibody (<a href="/products/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>) at 1/9,000 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/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>) at 1/9,000 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 HA723753, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded mouse liver tissue with Rabbit anti-SCD1 antibody (HA723753) at 1/9,000 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 (HA723753) at 1/9,000 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/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded rat adipose tissue with Rabbit anti-SCD1 antibody (<a href="/products/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>) at 1/9,000 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/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>) at 1/9,000 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 HA723753, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded rat adipose tissue with Rabbit anti-SCD1 antibody (HA723753) at 1/9,000 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 (HA723753) at 1/9,000 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/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded rat liver tissue with Rabbit anti-SCD1 antibody (<a href="/products/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>) at 1/9,000 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/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>) at 1/9,000 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 HA723753, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded rat liver tissue with Rabbit anti-SCD1 antibody (HA723753) at 1/9,000 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 (HA723753) at 1/9,000 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/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>, the same antibody clone in a different buffer formulation.<br />Flow cytometric analysis of MC/9 cells labeling SCD1.<br /><br />Cells were fixed and permeabilized. Then stained with the primary antibody (<a href="/products/HA723753" style="font-weight: bold;text-decoration: underline;">HA723753</a>, 1/1,000) (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).

    This data was developed using HA723753, the same antibody clone in a different buffer formulation.
    Flow cytometric analysis of MC/9 cells labeling SCD1.

    Cells were fixed and permeabilized. Then stained with the primary antibody (HA723753, 1/1,000) (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).

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