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ATP Citrate Lyase Antibody (YA596)

(Synonyms: ATP-citrate synthase, ATP-citrate (pro-S-)-lyase, Citrate cleavage enzyme, ACL, ACLY)
Customer Review

Based on 1 Customer Validation

ATP Citrate Lyase Antibody (YA596) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to ATP Citrate Lyase.

For research use only. We do not sell to patients.
  • Host:

    Rabbit

  • Isotype:

    IgG

  • Application:

    WB, ICC/IF, IHC-P, IP, FC

  • Reactivity :

    Human, Mouse

  • Formulation:

    Supplied in 1*TBS (pH7.4), 0.05% BSA and 40% Glycerol. Preservative: 0.05% Sodium Azide.

  • Conjugation:
    Non-conjugated
ALL WB FC ICC
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • ATP Citrate Lyase Antibody (YA596) Product Image
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To place orders, for customer services and technical support, please contact: MedChemExpress USA

Tel: 609-228-6898 E-mail: [email protected] [email protected]

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Related Products:
Top Publications Citing

Use of MCE Products

Applications

Application
WB Info
WB: Western Blot
ICC/IF Info
ICC/IF: Immunocytochemistry/
Immunofluorescence
IHC-P Info
IHC-P: Immunohistochemistry-Paraffin
FC Info
FC: Flow Cytometry
IP Info
IP: Immunoprecipitation
Dilution Ratio 1:500-1:2000 1:50-1:200 1:50-1:200 1:50-1:200 Use at an assay dependent concentration.

Product Details

Description

ATP Citrate Lyase Antibody (YA596) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to ATP Citrate Lyase.

  • Host Rabbit
  • Clonality Recombinant,Monoclonal
  • Species Reactivity
    Human, Mouse
  • Observed Molecular Weight
    Observed band size: 121 kDa Info
    Note: Due to possible protein modifications or aggregation, the molecular weight should be confirmed by actual measurement, and the predicted value is for reference only.
  • Calculated Molecular Weight Predicted band size: 121 kDa
Species Reactivity Database
Immunogen

Synthetic peptide within C-terminal human ATP citrate lyase.

Sensitivity

Endogenous

Purification

Protein A affinity purified.

Conjugation

Non-conjugated

Modification

Unmodified

Isotype

IgG

RRID

AB_3102468

Product Properties

  • Appearance

    Solution

  • Formulation

    Supplied in 1*TBS (pH7.4), 0.05% BSA and 40% Glycerol. Preservative: 0.05% Sodium Azide.

  • Concentration

    Batch-dependent, Please check the COA for the concentration of each lot. Check Lot Concentration

  • Storage & Stability

    Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.

  • Shipping

    Shipping with blue ice.

Verification Images

  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
    Western blot analysis was performed on protein extracts (25 μg) from Hela (lane 2), NIH/3T3 (lane 3), A549 (lane 4), A431 (lane 5), Jurkat (lane 6) and Raji (lane 7) using ATP Citrate Lyase antibody. Proteins were transferred onto a 0.22 μm PVDF membrane using a wet transfer system at a voltage of 100 V for 90 mins. The membrane was then blocked with 5% nonfat milk in TBST (HY-K1025) for 1 h at room temperature. The primary antibody (1:1000) and loading control antibody GAPDH Antibody (HRP) (HY-P80954A) (1:5000) were diluted in 5% nonfat milk in TBST and incubated with the membrane overnight at 4°C. After washing, the membrane of primary antibody was incubated with HRP-conjugated goat anti-rabbit/mouse IgG secondary antibody (HY-P8001/HY-P8004) (1:5000) diluted in 5% nonfat milk in TBST for 1 h at room temperature. Protein bands were visualized using an Ultra High Sensitivity ECL detection kit (HY-K1005).
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
    Western blot analysis of extracts from Hela(lane 2(20μg), NIH3T3(lane 3(20μg) and A549(lane 4(20μg) using ATP citrate lyase (HY-P80380) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in TBST for 2 hour at room temperature. The primary antibody (HY-P80380, 1/1000) and Loading control antibody (GAPDH, HY-P80954, 1/3000) was used in 5% BSA in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (HY-P8004/HY-P8001, 1/10,000) was used for 1 hour at room temperature.
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
    Flow cytometric analysis of 1X106 NIH-3T3 cells labeling ATP Citrate Lyase Antibody(HY-P80380, red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Then stained with the primary antibody at 1/100 dilution for an hour at 4℃. AF488-conjugated Goat Anti-Rabbit IgG H&L (HY-P8002) was used as the secondary antibody at 1/1,000 dilution for 30 minutes at 4℃. Rabbit IgG Isotype Control (HY-P80879, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
    Immunocytochemistry analysis of Hela cells labeling ATP Citrate Lyase with ATP Citrate Lyase Antibody (HY-P80380) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with quick block buffer for 10 minutes at room temperature. Cells were then incubated with ATP Citrate Lyase Antibody (HY-P80380) at 1/100 dilution in quick block buffer overnight at 4 ℃. AF488-conjugated Goat Anti-Rabbit IgG H&L（HY-P8002, Green） 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. The Nuclear counterstain was DAPI (Blue).
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
    Immunocytochemistry analysis of Hela cells labeling ATP Citrate Lyase with ATP Citrate Lyase Antibody (HY-P80380) at 1/200 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with quick block buffer for 10 minutes at room temperature. Cells were then incubated with ATP Citrate Lyase Antibody (HY-P80380) at 1/200 dilution in quick block buffer overnight at 4 ℃. AF488-conjugated Goat Anti-Rabbit IgG H&L（HY-P8002, Green） 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. The Nuclear counterstain was DAPI (Blue).

Background

  • Function

    ATP-citrate lyase (ACLY) is a central metabolic enzyme and catalyses the ATP-dependent conversion of citrate and coenzyme A (CoA) to oxaloacetate and acetyl-CoA. The acetyl-CoA product is crucial for the metabolism of fatty acids, the biosynthesis of cholesterol, and the acetylation and prenylation of proteins. Acetyl CoA is also required for acetylation reactions that modify proteins, such as histone acetylation. ACLY is upregulated or activated in several types of cancers, and its inhibition is known to induce proliferation arrest in cancer cells both in vitro and in vivo.

    ACLY links glucose and lipid metabolism by catalyzing the formation of acetyl-CoA and oxaloacetate from citrate produced by glycolysis in the presence of ATP and CoA. ACLY is aberrantly expressed in many immortalized cells and tumors, such as breast, liver, colon, lung and prostate cancers, and is correlated reversely with tumor stage and differentiation, serving as a negative prognostic marker. ACLY is an upstream enzyme of the long chain fatty acid synthesis, providing acetyl-CoA as an essential component of the fatty acid synthesis. Therefore, ACLY is a key enzyme of cellular lipogenesis and potent target for cancer therapy.

  • Subcellular Localization

    Cytoplasm, cytosol

  • Subunit

    Homotetramer

  • SwissProt ID

    P53396

  • Gene ID
    47 [NCBI]
  • Synonyms

    ATP-citrate synthase, ATP-citrate (pro-S-)-lyase, Citrate cleavage enzyme, ACL, ACLY

  • Research Field

    Signal Transduction

ATP Citrate Lyase Antibody (YA596) Related Classifications

MOQ
Minimum order quantity
100 mg

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Measured by its ability to inhibit anti-CD3-induced proliferation of stimulated CTLL-2 mouse cytotoxic T cells. The ED50 this effect is 0.8023 μg/ml, corresponding to a specific activity is 1246.42 units/mg.

Assay Types
  • 1/16

    MedChemExpress Validation
     Western blot analysis was performed on protein extracts (25 μg) from Hela (lane 2), NIH/3T3 (lane 3), A549 (lane 4), A431 (lane 5), Jurkat (lane 6) and Raji (lane 7) using ATP Citrate Lyase antibody. Proteins were transferred onto a 0.22 μm PVDF membrane using a wet transfer system at a voltage of 100 V for 90 mins. The membrane was then blocked with 5% nonfat milk in TBST (HY-K1025) for 1 h at room temperature. The primary antibody (1:1000) and loading control antibody GAPDH Antibody (HRP) (HY-P80954A) (1:5000) were diluted in 5% nonfat milk in TBST and incubated with the membrane overnight at 4°C. After washing, the membrane of primary antibody was incubated with HRP-conjugated goat anti-rabbit/mouse IgG secondary antibody (HY-P8001/HY-P8004) (1:5000) diluted in 5% nonfat milk in TBST for 1 h at room temperature. Protein bands were visualized using an Ultra High Sensitivity ECL detection kit (HY-K1005).

  • 1/16

    MedchemExpress Validation
     Western blot analysis of extracts from Hela(lane 2(20μg), NIH3T3(lane 3(20μg) and A549(lane 4(20μg) using ATP citrate lyase (HY-P80380) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in TBST for 2 hour at room temperature. The primary antibody (HY-P80380, 1/1000) and Loading control antibody (GAPDH, HY-P80954, 1/3000) was used in 5% BSA in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (HY-P8004/HY-P8001, 1/10,000) was used for 1 hour at room temperature.

  • 1/16

    MedChemExpress Validation
     Flow cytometric analysis of 1X106 NIH-3T3 cells labeling ATP Citrate Lyase Antibody(HY-P80380, red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Then stained with the primary antibody at 1/100 dilution for an hour at 4℃. AF488-conjugated Goat Anti-Rabbit IgG H&L (HY-P8002) was used as the secondary antibody at 1/1,000 dilution for 30 minutes at 4℃. Rabbit IgG Isotype Control (HY-P80879, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).

  • 1/16

    MedChemExpress Validation
     Immunocytochemistry analysis of Hela cells labeling ATP Citrate Lyase with ATP Citrate Lyase Antibody (HY-P80380) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with quick block buffer for 10 minutes at room temperature. Cells were then incubated with ATP Citrate Lyase Antibody (HY-P80380) at 1/100 dilution in quick block buffer overnight at 4 ℃. AF488-conjugated Goat Anti-Rabbit IgG H&L（HY-P8002, Green） 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. The Nuclear counterstain was DAPI (Blue).

  • 1/16

    MedChemExpress Validation
     Immunocytochemistry analysis of Hela cells labeling ATP Citrate Lyase with ATP Citrate Lyase Antibody (HY-P80380) at 1/200 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with quick block buffer for 10 minutes at room temperature. Cells were then incubated with ATP Citrate Lyase Antibody (HY-P80380) at 1/200 dilution in quick block buffer overnight at 4 ℃. AF488-conjugated Goat Anti-Rabbit IgG H&L（HY-P8002, Green） 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. The Nuclear counterstain was DAPI (Blue).

  • ATP Citrate Lyase Antibody (YA596) Product Image
    1/16
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • ATP Citrate Lyase Antibody (YA596) Product Image
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
    1/1
    MedChemExpress Validation
     Western blot analysis was performed on protein extracts (25 μg) from Hela (lane 2), NIH/3T3 (lane 3), A549 (lane 4), A431 (lane 5), Jurkat (lane 6) and Raji (lane 7) using ATP Citrate Lyase antibody. Proteins were transferred onto a 0.22 μm PVDF membrane using a wet transfer system at a voltage of 100 V for 90 mins. The membrane was then blocked with 5% nonfat milk in TBST (HY-K1025) for 1 h at room temperature. The primary antibody (1:1000) and loading control antibody GAPDH Antibody (HRP) (HY-P80954A) (1:5000) were diluted in 5% nonfat milk in TBST and incubated with the membrane overnight at 4°C. After washing, the membrane of primary antibody was incubated with HRP-conjugated goat anti-rabbit/mouse IgG secondary antibody (HY-P8001/HY-P8004) (1:5000) diluted in 5% nonfat milk in TBST for 1 h at room temperature. Protein bands were visualized using an Ultra High Sensitivity ECL detection kit (HY-K1005).
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
    1/1
    MedchemExpress Validation
     Western blot analysis of extracts from Hela(lane 2(20μg), NIH3T3(lane 3(20μg) and A549(lane 4(20μg) using ATP citrate lyase (HY-P80380) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in TBST for 2 hour at room temperature. The primary antibody (HY-P80380, 1/1000) and Loading control antibody (GAPDH, HY-P80954, 1/3000) was used in 5% BSA in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (HY-P8004/HY-P8001, 1/10,000) was used for 1 hour at room temperature.
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
    1/1
    MedChemExpress Validation
     Flow cytometric analysis of 1X106 NIH-3T3 cells labeling ATP Citrate Lyase Antibody(HY-P80380, red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Then stained with the primary antibody at 1/100 dilution for an hour at 4℃. AF488-conjugated Goat Anti-Rabbit IgG H&L (HY-P8002) was used as the secondary antibody at 1/1,000 dilution for 30 minutes at 4℃. Rabbit IgG Isotype Control (HY-P80879, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
    1/1
    MedChemExpress Validation
     Immunocytochemistry analysis of Hela cells labeling ATP Citrate Lyase with ATP Citrate Lyase Antibody (HY-P80380) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with quick block buffer for 10 minutes at room temperature. Cells were then incubated with ATP Citrate Lyase Antibody (HY-P80380) at 1/100 dilution in quick block buffer overnight at 4 ℃. AF488-conjugated Goat Anti-Rabbit IgG H&L（HY-P8002, Green） 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. The Nuclear counterstain was DAPI (Blue).
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
    1/1
    MedChemExpress Validation
     Immunocytochemistry analysis of Hela cells labeling ATP Citrate Lyase with ATP Citrate Lyase Antibody (HY-P80380) at 1/200 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with quick block buffer for 10 minutes at room temperature. Cells were then incubated with ATP Citrate Lyase Antibody (HY-P80380) at 1/200 dilution in quick block buffer overnight at 4 ℃. AF488-conjugated Goat Anti-Rabbit IgG H&L（HY-P8002, Green） 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. The Nuclear counterstain was DAPI (Blue).
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • Experimental Validation Results for ATP Citrate Lyase Antibody (YA596)
  • ATP Citrate Lyase Antibody (YA596) Product Image
    MedChemExpress Validation

    Western blot analysis was performed on protein extracts (25 μg) from Hela (lane 2), NIH/3T3 (lane 3), A549 (lane 4), A431 (lane 5), Jurkat (lane 6) and Raji (lane 7) using ATP Citrate Lyase antibody. Proteins were transferred onto a 0.22 μm PVDF membrane using a wet transfer system at a voltage of 100 V for 90 mins. The membrane was then blocked with 5% nonfat milk in TBST (HY-K1025) for 1 h at room temperature. The primary antibody (1:1000) and loading control antibody GAPDH Antibody (HRP) (HY-P80954A) (1:5000) were diluted in 5% nonfat milk in TBST and incubated with the membrane overnight at 4°C. After washing, the membrane of primary antibody was incubated with HRP-conjugated goat anti-rabbit/mouse IgG secondary antibody (HY-P8001/HY-P8004) (1:5000) diluted in 5% nonfat milk in TBST for 1 h at room temperature. Protein bands were visualized using an Ultra High Sensitivity ECL detection kit (HY-K1005).

  • ATP Citrate Lyase Antibody (YA596) Product Image
    MedchemExpress Validation

    Western blot analysis of extracts from Hela(lane 2(20μg), NIH3T3(lane 3(20μg) and A549(lane 4(20μg) using ATP citrate lyase (HY-P80380) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in TBST for 2 hour at room temperature. The primary antibody (HY-P80380, 1/1000) and Loading control antibody (GAPDH, HY-P80954, 1/3000) was used in 5% BSA in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (HY-P8004/HY-P8001, 1/10,000) was used for 1 hour at room temperature.

  • ATP Citrate Lyase Antibody (YA596) Product Image
    MedChemExpress Validation

    Flow cytometric analysis of 1X106 NIH-3T3 cells labeling ATP Citrate Lyase Antibody(HY-P80380, red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Then stained with the primary antibody at 1/100 dilution for an hour at 4℃. AF488-conjugated Goat Anti-Rabbit IgG H&L (HY-P8002) was used as the secondary antibody at 1/1,000 dilution for 30 minutes at 4℃. Rabbit IgG Isotype Control (HY-P80879, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).

  • ATP Citrate Lyase Antibody (YA596) Product Image
    MedChemExpress Validation

    Immunocytochemistry analysis of Hela cells labeling ATP Citrate Lyase with ATP Citrate Lyase Antibody (HY-P80380) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with quick block buffer for 10 minutes at room temperature. Cells were then incubated with ATP Citrate Lyase Antibody (HY-P80380) at 1/100 dilution in quick block buffer overnight at 4 ℃. AF488-conjugated Goat Anti-Rabbit IgG H&L（HY-P8002, Green） 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. The Nuclear counterstain was DAPI (Blue).

  • ATP Citrate Lyase Antibody (YA596) Product Image
    MedChemExpress Validation

    Immunocytochemistry analysis of Hela cells labeling ATP Citrate Lyase with ATP Citrate Lyase Antibody (HY-P80380) at 1/200 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with quick block buffer for 10 minutes at room temperature. Cells were then incubated with ATP Citrate Lyase Antibody (HY-P80380) at 1/200 dilution in quick block buffer overnight at 4 ℃. AF488-conjugated Goat Anti-Rabbit IgG H&L（HY-P8002, Green） 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. The Nuclear counterstain was DAPI (Blue).

  • ATP Citrate Lyase Antibody (YA596) Product Image WB
  • ATP Citrate Lyase Antibody (YA596) Product Image WB
  • ATP Citrate Lyase Antibody (YA596) Product Image FC
  • ATP Citrate Lyase Antibody (YA596) Product Image ICC
  • ATP Citrate Lyase Antibody (YA596) Product Image ICC