Glucokinase Recombinant Rabbit Monoclonal Antibody [PSH28-07]
cat.: HA752094
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Mouse, Rat
Applications: WB, IHC-P, IF-Tissue, IP
Clonality: Monoclonal
Clone number: PSH28-07
Form: Liquid
Storage condition: Store at 2-8℃. Avoid freeze.
Storage buffer: PBS (pH7.4).
Concentration: 0.5ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 52 kDa
Isotype: IgG
Immunogen: Recombinant protein within mouse Glucokinase aa 1-465.
Positive control: Mouse liver tissue lysate, Rat liver tissue lysate.
Subcellular location: Cytoplasm, Nucleus, Mitochondrion.
Uniprot #: SwissProt: P52792 Mouse | P17712 Rat
Alternative names: ATP:D-hexose 6-phosphotransferase FGQTL3 GCK GK GLK Glucokinase Hexokinase D pancreatic isozyme Hexokinase type IV Hexokinase-4 Hexokinase-D HHF3 HK IV HK4 HKIV HXK4_HUMAN HXKP LGLK MODY2
Images
HA752094_1.jpg Fig1: This data was developed using HA752094, the same antibody clone in a different buffer formulation.
Western blot analysis of Glucokinase on different lysates with Rabbit anti-Glucokinase antibody (HA752094) at 1/2,500 dilution.

Lane 1: Mouse liver tissue lysate
Lane 2: Mouse kidney tissue lysate
Lane 3: Mouse skeletal muscle tissue lysate
Lane 4: Rat liver tissue lysate
Lane 5: Rat kidney tissue lysate
Lane 6: Rat skeletal muscle tissue lysate

Lysates/proteins at 20 µg/Lane.
Exposure time: 8 seconds; ECL: K1801

Low expression: skeletal muscle (PMID: 23085254).
Low expression of Glucokinase protein in kidney is consistent with the predicted expression pattern.

Blocking: 5% NFDM/TBST, 1 hour at room temperature
Primary antibody: HA752094, 1/2,500 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: 52 kDa
Observed band size: 52 kDa
HA752094_2.jpg Fig2: This data was developed using HA752094, the same antibody clone in a different buffer formulation.
Western blot analysis of Glucokinase on different lysates with Rabbit anti-Glucokinase antibody (HA752094) at 1/2,500 dilution.

Lane 1: His-tagged Human Glucokinase recombinant protein
Lane 2: His-tagged Human Hexokinase II recombinant protein

Lysates/proteins at 10 ng/Lane.
Exposure time: 4 seconds; ECL: K1801

Blocking: 5% NFDM/TBST, 1 hour at room temperature
Primary antibody: HA752094, 1/2,500 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: 52 kDa
Observed band size: 52 kDa
HA752094_3.jpg Fig3: This data was developed using HA752094, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

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

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

Liver tissue from fasted mice. At low glucose concentrations, GCK binds to GCKR, and the resulting inactive complex is recruited into the hepatocyte nucleus (PMID: 24566088, PMID: 10713097).

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: HA752094, 1/5,000, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.
HA752094_4.jpg Fig4: This data was developed using HA752094, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Mouse
Tissue: Kidney
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: HA752094, 1/5,000, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.

Low expression of Glucokinase protein in kidney is consistent with the predicted expression pattern.
HA752094_5.jpg Fig5: This data was developed using HA752094, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

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

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

Liver tissue from fasted rats. At low glucose concentrations, GCK binds to GCKR, and the resulting inactive complex is recruited into the hepatocyte nucleus (PMID: 24566088, PMID: 10713097).

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: HA752094, 1/5,000, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.
HA752094_6.jpg Fig6: This data was developed using HA752094, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Rat
Tissue: Kidney
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: HA752094, 1/5,000, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.

Low expression of Glucokinase protein in kidney is consistent with the predicted expression pattern.
HA752094_7.jpg Fig7: This data was developed using HA752094, the same antibody clone in a different buffer formulation.
Application: Immunofluorescence (IF-tissue)

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

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

Liver tissue from fasted mice. At low glucose concentrations, GCK binds to GCKR, and the resulting inactive complex is recruited into the hepatocyte nucleus (PMID: 24566088, PMID: 10713097).

Wash buffer: 1× TBST
Blocking: 10% normal goat serum + 1% Triton X-100 + 0.3 M Glycine in TBST, 30 minutes at room temperature.
Primary antibody: HA752094, 1/500, overnight at 4℃.
Secondary antibody: Goat Anti-Rabbit IgG (iFluor™ 488, HA1121), 1.5 hours at room temperature.
HA752094_8.jpg Fig8: This data was developed using HA752094, the same antibody clone in a different buffer formulation.
Application: Immunofluorescence (IF-tissue)

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

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

Liver tissue from fasted rats. At low glucose concentrations, GCK binds to GCKR, and the resulting inactive complex is recruited into the hepatocyte nucleus (PMID: 24566088, PMID: 10713097).

Wash buffer: 1× TBST
Blocking: 10% normal goat serum + 1% Triton X-100 + 0.3 M Glycine in TBST, 30 minutes at room temperature.
Primary antibody: HA752094, 1/500, overnight at 4℃.
Secondary antibody: Goat Anti-Rabbit IgG (iFluor™ 488, HA1121), 1.5 hours at room temperature.
HA752094_9.jpg Fig9: This data was developed using HA752094, the same antibody clone in a different buffer formulation.
Immunoprecipitation (IP)

Glucokinase was immunoprecipitated in 0.2 mg Mouse liver tissue lysate with HA752094 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using HA752094 at 1/2,500 dilution. Anti-Rabbit IgG for IP, AlpSdAbs® VHH(HRP) (025-100-005) at 1/5,000 dilution was used for 1 hour at room temperature.

Lane 1: Mouse liver tissue lysate (input)
Lane 2: HA752094 IP in mouse tissue cell lysate
Lane 3: Rabbit IgG instead of HA752094 in mouse liver tissue lysate

Exposure time: 10 seconds
Blocking: 5% NFDM/TBST, 1 hour at room temperature

Primary dilution: HA752094, 1/2,500 in primary antibody dilution buffer (K1803), 2 hours at room temperature

Predicted band size: 52 kDa
Observed band size: 52 kDa
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.