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GBE1 Antibody (YA7798)

(Synonyms: APBD; GBE; GSD4)

GBE1 Antibody (YA7798) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to GBE1.

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

    Mouse

  • Isotype:

    IgG1

  • Application:

    WB, ICC/IF, IP, FC

  • Reactivity :

    Human, Mouse, Rat

  • Formulation:

    Spplied in PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

  • Conjugation:
    Non-conjugated
ALL WB ICC
  • Experimental Validation Results for GBE1 Antibody (YA7798)
  • Experimental Validation Results for GBE1 Antibody (YA7798)
  • Experimental Validation Results for GBE1 Antibody (YA7798)
  • GBE1 Antibody (YA7798) 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:
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Use of MCE Products

Applications

Application
WB Info
WB: Western Blot
ICC/IF Info
ICC/IF: Immunocytochemistry/
Immunofluorescence
FC Info
FC: Flow Cytometry
IP Info
IP: Immunoprecipitation
Dilution Ratio 1:2000-3000 1:50-100 1:100 2ug/500ul

Product Details

Description

GBE1 Antibody (YA7798) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to GBE1.

  • Host Mouse
  • Clonality Monoclonal
  • Species Reactivity
    Human, Mouse, Rat
  • Calculated Molecular Weight Predicted band size: 80.3 kDa
Immunogen

Full length human recombinant protein of human GBE1 produced in HEK293T cell.

Sensitivity

Endogenous

Purification

Affinity purified

Conjugation

Non-conjugated

Modification

Unmodified

Isotype

IgG1

Product Properties

  • Appearance

    Solution

  • Formulation

    Spplied in PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% 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 GBE1 Antibody (YA7798)
    Western blot analysis of extracts from Rat liver tissue(lane 2(20μg) , Mouse liver tissue(lane 3(20μg) ,HL-60(lane 4(20μg)and HepG2( lane 5(20μg) using GBE1 Antibody (HY-P88114). Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/2000) and Loading control antibody (Beta Actin, HY-P80993，1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse IgG-HRP Secondary Antibody (HY-P8004,1/10,000) was used for 1 hour at room temperature.
  • Experimental Validation Results for GBE1 Antibody (YA7798)
    Immunocytochemistry analysis of Hela cells labeling GBE1 with GBE1 Antibody (HY-P88114) 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 GBE1 Antibody (HY-P88114) at 1/100 dilution in quick block buffer overnight at 4 ℃.AF488-conjugated Goat Anti-Mouse IgG H&L（HY-P8005, 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 GBE1 Antibody (YA7798)
    Immunocytochemistry analysis of PC-3 cells labeling GBE1 with GBE1 Antibody (HY-P88114) 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 GBE1 Antibody (HY-P88114) at 1/100 dilution in quick block buffer overnight at 4 ℃.AF488-conjugated Goat Anti-Mouse IgG H&L（HY-P8005, 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

    GBE1 is a Glycogen-branching enzyme participates in the glycogen biosynthetic process along with glycogenin and glycogen synthase. Generates alpha-1,6-glucosidic branches from alpha-1,4-linked glucose chains, to increase solubility of the glycogen polymer[1][2][3].

  • Isoforms & Post-Translational Modification

    Q04446: 702 amino acids, molecular weight 80474 Da.

  • Subunit

    Monomer

  • SwissProt ID

    Q04446

  • Synonyms

    APBD; GBE; GSD4

GBE1 Antibody (YA7798) 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 of extracts from Rat liver tissue(lane 2(20μg) , Mouse liver tissue(lane 3(20μg) ,HL-60(lane 4(20μg)and HepG2( lane 5(20μg) using GBE1 Antibody (HY-P88114). Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/2000) and Loading control antibody (Beta Actin, HY-P80993，1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse IgG-HRP Secondary Antibody (HY-P8004,1/10,000) was used for 1 hour at room temperature.

  • 1/16

    MedChemExpress Validation
     Immunocytochemistry analysis of Hela cells labeling GBE1 with GBE1 Antibody (HY-P88114) 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 GBE1 Antibody (HY-P88114) at 1/100 dilution in quick block buffer overnight at 4 ℃.AF488-conjugated Goat Anti-Mouse IgG H&L（HY-P8005, 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 PC-3 cells labeling GBE1 with GBE1 Antibody (HY-P88114) 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 GBE1 Antibody (HY-P88114) at 1/100 dilution in quick block buffer overnight at 4 ℃.AF488-conjugated Goat Anti-Mouse IgG H&L（HY-P8005, 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).

  • GBE1 Antibody (YA7798) Product Image
    1/16
  • Experimental Validation Results for GBE1 Antibody (YA7798)
  • Experimental Validation Results for GBE1 Antibody (YA7798)
  • Experimental Validation Results for GBE1 Antibody (YA7798)
  • GBE1 Antibody (YA7798) Product Image
  • Experimental Validation Results for GBE1 Antibody (YA7798)
    1/1
    MedChemExpress Validation
     Western blot analysis of extracts from Rat liver tissue(lane 2(20μg) , Mouse liver tissue(lane 3(20μg) ,HL-60(lane 4(20μg)and HepG2( lane 5(20μg) using GBE1 Antibody (HY-P88114). Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/2000) and Loading control antibody (Beta Actin, HY-P80993，1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse IgG-HRP Secondary Antibody (HY-P8004,1/10,000) was used for 1 hour at room temperature.
  • Experimental Validation Results for GBE1 Antibody (YA7798)
    1/1
    MedChemExpress Validation
     Immunocytochemistry analysis of Hela cells labeling GBE1 with GBE1 Antibody (HY-P88114) 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 GBE1 Antibody (HY-P88114) at 1/100 dilution in quick block buffer overnight at 4 ℃.AF488-conjugated Goat Anti-Mouse IgG H&L（HY-P8005, 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 GBE1 Antibody (YA7798)
    1/1
    MedChemExpress Validation
     Immunocytochemistry analysis of PC-3 cells labeling GBE1 with GBE1 Antibody (HY-P88114) 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 GBE1 Antibody (HY-P88114) at 1/100 dilution in quick block buffer overnight at 4 ℃.AF488-conjugated Goat Anti-Mouse IgG H&L（HY-P8005, 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 GBE1 Antibody (YA7798)
  • Experimental Validation Results for GBE1 Antibody (YA7798)
  • Experimental Validation Results for GBE1 Antibody (YA7798)
  • GBE1 Antibody (YA7798) Product Image
    MedChemExpress Validation

    Western blot analysis of extracts from Rat liver tissue(lane 2(20μg) , Mouse liver tissue(lane 3(20μg) ,HL-60(lane 4(20μg)and HepG2( lane 5(20μg) using GBE1 Antibody (HY-P88114). Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/2000) and Loading control antibody (Beta Actin, HY-P80993，1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse IgG-HRP Secondary Antibody (HY-P8004,1/10,000) was used for 1 hour at room temperature.

  • GBE1 Antibody (YA7798) Product Image
    MedChemExpress Validation

    Immunocytochemistry analysis of Hela cells labeling GBE1 with GBE1 Antibody (HY-P88114) 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 GBE1 Antibody (HY-P88114) at 1/100 dilution in quick block buffer overnight at 4 ℃.AF488-conjugated Goat Anti-Mouse IgG H&L（HY-P8005, 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).

  • GBE1 Antibody (YA7798) Product Image
    MedChemExpress Validation

    Immunocytochemistry analysis of PC-3 cells labeling GBE1 with GBE1 Antibody (HY-P88114) 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 GBE1 Antibody (HY-P88114) at 1/100 dilution in quick block buffer overnight at 4 ℃.AF488-conjugated Goat Anti-Mouse IgG H&L（HY-P8005, 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).

  • GBE1 Antibody (YA7798) Product Image WB
  • GBE1 Antibody (YA7798) Product Image ICC
  • GBE1 Antibody (YA7798) Product Image ICC