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ADX Recombinant Rabbit Monoclonal Antibody [JE63-56] - BSA and Azide free

Usd: 649

Specification

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Catalog# HA752023

ADX Recombinant Rabbit Monoclonal Antibody [JE63-56] - BSA and Azide free

Application

  • WB

  • IHC-P

  • IF-Cell

Reactivity

  • Human

  • Mouse

  • Rat

With BSA and Azide
Conjugation

  • unconjugated

Overview

Product Name

ADX Recombinant Rabbit Monoclonal Antibody [JE63-56] - BSA and Azide free

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Synthetic peptide within Human ADX aa 51-100 / 184.

Species Reactivity

Human, Mouse, Rat

Validated Applications

WB, IHC-P, IF-Cell

Target Molecular Weight

Predicted band size: 19 kDa

Positive Control

SK-Br-3 cell lysate, K-562 cell lysate, HepG2 cell lysate, 293T cell lysate, Rat liver tissue lysate, Rat testis tissue lysate, Rat kidney tissue lysate, Mouse liver tissue lysate, PC-12, human placenta tissue, rat adrenal gland tissue.

Conjugation

unconjugated

Clone Number

JE63-56

Reactivity Data

Tested Tested Tested
Verified (internally validated)
Published Tested
Reported in literature (not internally validated)
Predicted Tested
Predicted reactive (based on sequence homology)
Not recommended Tested
Not recommended (failed internal validation)
WB IHC-P IF-Cell
human
Tested Tested
Tested Tested
 
mouse
Tested Tested
 
 
rat
Tested Tested
Tested Tested
Tested Tested

Product Features

Form

Liquid

Concentration

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

Storage Instructions

Store at 2-8℃. Avoid freeze.

Storage Buffer

PBS (pH7.4).

Isotype

IgG

Purification Method

Protein A affinity purified.

Application Dilution

Target

Function

Adrenal ferredoxin (also adrenodoxin (ADX), adrenodoxin, mitochondrial, hepatoredoxin, ferredoxin-1 (FDX1)) is a protein that in humans is encoded by the FDX1 gene. In addition to the expressed gene at this chromosomal locus (11q22), there are pseudogenes located on chromosomes 20 and 21. Adrenodoxin is a small iron-sulfur protein that can accept and carry a single electron. Adrenodoxin functions as an electron transfer protein in the mitochondrial cytochrome P450 systems. The first enzyme in this system is adrenodoxin reductase that carries an FAD. FAD can be reduced by two electrons donated from coenzyme NADPH. These two electrons are transferred one a time to adrenodoxin. Adrenodoxin in return reduces mitochondrial cytochrome P450. This particular oxidation/reduction system is involved in the synthesis of steroid hormones in steroidogenic tissues. In addition, similar systems also function in vitamin D and bile acid synthesis in the kidney and liver respectively. Adrenodoxin has been identified in a number of different tissues but all forms have been shown to be identical and are not tissue specific.

Background References

1. Zhang Z et al. FDX1 can Impact the Prognosis and Mediate the Metabolism of Lung Adenocarcinoma. Front Pharmacol. 2021 Oct

2. Wang Z et al. The role of FDX1 in granulosa cell of Polycystic ovary syndrome (PCOS). BMC Endocr Disord. 2021 Jun

Subcellular Location

Mitochondrion matrix.

UNIPROT

SwissProt: P10109 Human

SwissProt: P46656 Mouse

SwissProt: P24483 Rat

Synonyms

Adrenal ferredoxin antibody

Adrenodoxin antibody

Adrenodoxin, mitochondrial antibody

ADX antibody

ADX_HUMAN antibody

FDX antibody

fdx1 antibody

Ferredoxin 1 antibody

Ferredoxin-1 antibody

Hepatoredoxin antibody

Expand

Images

  • This data was developed using <a href="/products/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>, the same antibody clone in a different buffer formulation.<br />Western blot analysis of ADX on different lysates with Rabbit anti-ADX antibody (<a href="/products/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>) at 1/500 dilution.<br /><br />Lane 1: SK-Br-3 cell lysate (15 µg/Lane)<br />Lane 2: K-562 cell lysate (15 µg/Lane)<br />Lane 3: HepG2 cell lysate (15 µg/Lane)<br />Lane 4: 293T cell lysate (15 µg/Lane)<br /><br />Predicted band size: 19 kDa<br />Observed band size: 13 kDa<br /><br />Exposure time: 5 minutes;<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/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (<a href="/products/HA1001" style="font-weight: bold;text-decoration: underline;">HA1001</a>) at 1:200,000 dilution was used for 1 hour at room temperature.

    This data was developed using HA721329, the same antibody clone in a different buffer formulation.
    Western blot analysis of ADX on different lysates with Rabbit anti-ADX antibody (HA721329) at 1/500 dilution.

    Lane 1: SK-Br-3 cell lysate (15 µg/Lane)
    Lane 2: K-562 cell lysate (15 µg/Lane)
    Lane 3: HepG2 cell lysate (15 µg/Lane)
    Lane 4: 293T cell lysate (15 µg/Lane)

    Predicted band size: 19 kDa
    Observed band size: 13 kDa

    Exposure time: 5 minutes;

    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 (HA721329) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.

  • This data was developed using <a href="/products/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>, the same antibody clone in a different buffer formulation.<br />Western blot analysis of ADX on different lysates with Rabbit anti-ADX antibody (<a href="/products/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>) at 1/500 dilution.<br /><br />Lane 1: Rat liver tissue lysate (40 µg/Lane)<br />Lane 2: Rat testis tissue lysate (40 µg/Lane)<br />Lane 3: Rat kidney tissue lysate (40 µg/Lane)<br />Lane 4: SK-Br-3 cell lysate (40 µg/Lane)<br /><br />Predicted band size: 19 kDa<br />Observed band size: 13 kDa<br /><br />Exposure time: 2 minutes; 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/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. 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 HA721329, the same antibody clone in a different buffer formulation.
    Western blot analysis of ADX on different lysates with Rabbit anti-ADX antibody (HA721329) at 1/500 dilution.

    Lane 1: Rat liver tissue lysate (40 µg/Lane)
    Lane 2: Rat testis tissue lysate (40 µg/Lane)
    Lane 3: Rat kidney tissue lysate (40 µg/Lane)
    Lane 4: SK-Br-3 cell lysate (40 µg/Lane)

    Predicted band size: 19 kDa
    Observed band size: 13 kDa

    Exposure time: 2 minutes; 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 (HA721329) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. 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/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>, the same antibody clone in a different buffer formulation.<br />Western blot analysis of ADX on different lysates with Rabbit anti-ADX antibody (<a href="/products/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>) at 1/1,000 dilution.<br /><br />Lane 1: Mouse liver tissue lysate<br />Lane 2: Rat liver tissue lysate<br /><br />Lysates/proteins at 40 µg/Lane.<br /><br />Predicted band size: 19 kDa<br />Observed band size: 13 kDa<br /><br />Exposure time: 10 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/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>) at 1/1,000 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 HA721329, the same antibody clone in a different buffer formulation.
    Western blot analysis of ADX on different lysates with Rabbit anti-ADX antibody (HA721329) at 1/1,000 dilution.

    Lane 1: Mouse liver tissue lysate
    Lane 2: Rat liver tissue lysate

    Lysates/proteins at 40 µg/Lane.

    Predicted band size: 19 kDa
    Observed band size: 13 kDa

    Exposure time: 10 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 (HA721329) at 1/1,000 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/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>, the same antibody clone in a different buffer formulation.<br />Immunocytochemistry analysis of PC-12 cells labeling ADX with Rabbit anti-ADX antibody (<a href="/products/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>) at 1/50 dilution.<br /><br />Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-ADX antibody (<a href="/products/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>) at 1/50 dilution in 2% negative goat serum 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.

    This data was developed using HA721329, the same antibody clone in a different buffer formulation.
    Immunocytochemistry analysis of PC-12 cells labeling ADX with Rabbit anti-ADX antibody (HA721329) at 1/50 dilution.

    Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-ADX antibody (HA721329) at 1/50 dilution in 2% negative goat serum 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.

  • This data was developed using <a href="/products/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded human placenta tissue with Rabbit anti-ADX antibody (<a href="/products/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>) at 1/200 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/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</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.

    This data was developed using HA721329, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded human placenta tissue with Rabbit anti-ADX antibody (HA721329) at 1/200 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 (HA721329) 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.

  • This data was developed using <a href="/products/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded rat adrenal gland tissue with Rabbit anti-ADX antibody (<a href="/products/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</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/HA721329" style="font-weight: bold;text-decoration: underline;">HA721329</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.

    This data was developed using HA721329, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded rat adrenal gland tissue with Rabbit anti-ADX antibody (HA721329) 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 (HA721329) 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.

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