GATA4 Recombinant Rabbit Monoclonal Antibody [PSH23-98]

Overview

Product Name

GATA4 Recombinant Rabbit Monoclonal Antibody [PSH23-98] - BSA and Azide free

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Recombinant protein within human GATA4 aa 1-442.

Species Reactivity

Human, Mouse, Rat

Validated Applications

WB, IF-Cell, IHC-P, FC(Intra)

Target Molecular Weight

Predicted band size: 45 kDa

Positive Control

Hep G2 (Human liver cancer cells) cell lysate, NIH/3T3 (Mouse fibroblasts) cell lysate, Mouse ovary tissue lysate, Rat testis tissue lysate, Rat ovary tissue lysate.

Conjugation

unconjugated

Clone Number

PSH23-98

Reactivity Data

Tested

Verified (internally validated) Published

Reported in literature (not internally validated) Predicted

Predicted reactive (based on sequence homology) Not recommended

Not recommended (failed internal validation)

	WB	IF-Cell	IHC-P	FC(Intra)
Human
Mouse
Rat

Product Features

Form

Liquid

Concentration

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

Lot Concentration Lookup

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

Members of the GATA family share a conserved zinc finger DNA-binding domain and are capable of binding the WGATAR consensus sequence. GATA-1 is erythroid-specific and is responsible for the regulated transcription of erythroid genes. It is an essential component in the generation of the erythroid lineage. GATA-2 is expressed in embryonic brain and liver, HeLa and endothelial cells, as well as in erythroid cells. Studies with a modified GATA consensus sequence, AGATCTTA, have shown that GATA-2 and GATA-3 recognize this mutated consensus while GATA-1 has poor recognition of this sequence. This indicates broader regulatory capabilities of GATA-2 and GATA-3 than GATA-1. GATA-3 is highly expressed in T lymphocytes. GATA-4, GATA-5 and GATA-6 comprise a subfamily of transcription factors. Both GATA-4 and GATA-6 are found in heart, pancreas and ovary; lung and liver tissues exhibit GATA-6, but not GATA-4 expression. GATA-5 expression has been observed in differentiated heart and gut tissues and is present throughout the course of development in the heart. Although expression patterns of the various GATA transcription factors may overlap, it is not yet apparent how the GATA factors are able to discriminate in binding their appropriate target sites.

Background References

1. Yamada Y et al. Cardiac Reprogramming and Gata4 Overexpression Reduce Fibrosis and Improve Diastolic Dysfunction in Heart Failure With Preserved Ejection Fraction. Circulation. 2025 Feb

2. Zhou BR et al. Structural insights into the cooperative nucleosome recognition and chromatin opening by FOXA1 and GATA4. Mol Cell. 2024 Aug

Subcellular Location

Nucleus

UNIPROT

SwissProt: P43694 Human

SwissProt: Q08369 Mouse

SwissProt: P46152 Rat

Synonyms

ASD2 antibody

GATA 4 antibody

GATA binding protein 4 antibody

GATA-binding factor 4 antibody

gata4 antibody

GATA4_HUMAN antibody

MGC126629 antibody

Transcription factor GATA 4 antibody

Transcription factor GATA-4 antibody

Transcription factor GATA4 antibody

Expand

Images

☑ Relative expression (RE)

This data was developed using HA724409, the same antibody clone in a different buffer formulation.
Western blot analysis of GATA4 on different lysates with Rabbit anti-GATA4 antibody (HA724409) at 1/5,000 dilution.

Lane 1: Hep G2 (Human liver cancer cells) cell lysate
Lane 2: HeLa (Human cervical adenocarcinoma cells) cell lysate
Lane 3: NIH/3T3 (Mouse fibroblasts) cell lysate

Lysates/proteins at 15 µg/Lane.
Exposure time: 2 minutes; ECL: K1802

HeLa is a negative control (PMID: 24696446).

Blocking: 5% NFDM/TBST, 1 hour at room temperature
Primary antibody: HA724409, 1/5,000 in primary antibody dilution buffer (K1803), overnight at 4 °C
Secondary antibody: Goat anti-Rabbit IgG-HRP (HA1001), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature

Predicted band size: 45 kDa
Observed band size: 50 kDa
☑ Relative expression (RE)

This data was developed using HA724409, the same antibody clone in a different buffer formulation.
Western blot analysis of GATA4 on different lysates with Rabbit anti-GATA4 antibody (HA724409) at 1/5,000 dilution.

Lane 1: Mouse ovary tissue lysate
Lane 2: Mouse skeletal muscle tissue lysate

Lysates/proteins at 30 µg/Lane.
Exposure time: 25 seconds; ECL: K1801

Skeletal muscle tissue is a negative control (PMID: 22808244).

Blocking: 5% NFDM/TBST, 1 hour at room temperature
Primary antibody: HA724409, 1/5,000 in primary antibody dilution buffer (K1803), overnight at 4 °C
Secondary antibody: Goat anti-Rabbit IgG-HRP (HA1001), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature

Predicted band size: 45 kDa
Observed band size: 50 kDa
☑ Relative expression (RE)

This data was developed using HA724409, the same antibody clone in a different buffer formulation.
Western blot analysis of GATA4 on different lysates with Rabbit anti-GATA4 antibody (HA724409) at 1/2,000 dilution.

Lane 1: Rat testis tissue lysate
Lane 2: Rat ovary tissue lysate
Lane 3: Rat skeletal muscle tissue lysate

Lysates/proteins at 30 µg/Lane.
Exposure time: 1 minute; ECL: K1801

Skeletal muscle tissue is a negative control (PMID: 22808244).

Blocking: 5% NFDM/TBST, 1 hour at room temperature
Primary antibody: HA724409, 1/2,000 in primary antibody dilution buffer (K1803), overnight at 4 °C
Secondary antibody: Goat anti-Rabbit IgG-HRP (HA1001), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature

Predicted band size: 45 kDa
Observed band size: 50 kDa
This data was developed using HA724409, the same antibody clone in a different buffer formulation.
Application: Immunocytochemistry (IF-cell)

Species: Human
Sample: Hep G2 (Human liver cancer cells)

Fixation: 4% Paraformaldehyde, 15 minutes at room temperature.
Permeabilization: 0.1% Triton X-100, 15 minutes at room temperature.

Blocking: 1% BSA + 10% normal goat serum, 1 hour at room temperature.
Antibody dilution buffer: 1% BSA in PBST.
Primary antibody: HA724409, 1/100, overnight at 4°C.
Secondary antibody: Goat Anti-Rabbit IgG (iFluor™ 488, HA1121), 45 minutes at room temperature.

Counterstain: Beta tubulin (HA601187, red), 1/100, overnight at 4℃. The Nuclear counterstain was DAPI (Blue).
This data was developed using HA724409, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Human
Tissue: Testis
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C.

Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: HA724409, 1/200, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.
☑ Relative expression (RE)

This data was developed using HA724409, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Human
Tissue: Skeletal muscle
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C.

Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: HA724409, 1/200, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.

Skeletal muscle tissue is a negative control (PMID：22808244).
This data was developed using HA724409, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Mouse
Tissue: Testis
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C.

Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: HA724409, 1/200, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.
☑ Relative expression (RE)

This data was developed using HA724409, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Mouse
Tissue: Skeletal muscle
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C.

Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: HA724409, 1/200, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.

Skeletal muscle tissue is a negative control (PMID：22808244).
This data was developed using HA724409, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Rat
Tissue: Testis
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C.

Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: HA724409, 1/200, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.
☑ Relative expression (RE)

This data was developed using HA724409, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Rat
Tissue: Skeletal muscle
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C.

Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: HA724409, 1/200, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.

Skeletal muscle tissue is a negative control (PMID：22808244).
This data was developed using HA724409, the same antibody clone in a different buffer formulation.
Application: Flow Cytometry (Intra)

Species: Human
Sample: Hep G2 (Human liver cancer cells)

Fixation: 4% Paraformaldehyde, 15 minutes at room temperature.
Permeabilization: 1x Permeabilization Buffer (eBioscience), 15 minutes at room temperature.

Blocking: 1% BSA + 10% normal goat serum, 15 minutes at room temperature.
Antibody dilution buffer: 1x PBS.
Primary antibody: HA724409 (1/1,000) (Red) compared with Rabbit IgG Isotype Control (HA722127, Green), 15 minutes at room temperature.
Secondary antibody: Goat Anti-Rabbit IgG (iFluor™ 488, HA1121), 15 minutes at room temperature.
This data was developed using HA724409, the same antibody clone in a different buffer formulation.
Application: Flow Cytometry (Intra)

Species: Mouse
Sample: NIH/3T3 (Mouse fibroblasts)

Fixation: 4% Paraformaldehyde, 15 minutes at room temperature.
Permeabilization: 1x Permeabilization Buffer (eBioscience), 15 minutes at room temperature.

Blocking: 1% BSA + 10% normal goat serum, 15 minutes at room temperature.
Antibody dilution buffer: 1x PBS.
Primary antibody: HA724409 (1/1,000) (Red) compared with Rabbit IgG Isotype Control (HA722127, Green), 15 minutes at room temperature.
Secondary antibody: Goat Anti-Rabbit IgG (iFluor™ 488, HA1121), 15 minutes at room temperature.