Rabbit Recombinant Monoclonal Aldolase C antibody. Carrier free. Suitable for WB, IHC-P, ICC, I-ELISA and reacts with Human, Mouse, Rat, Synthetic peptide - Human samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
WB | IHC-P | IHC-Fr | ICC | Flow Cyt (Intra) | IP | I-ELISA | |
---|---|---|---|---|---|---|---|
Human | Tested | Tested | Not recommended | Expected | Not recommended | Not recommended | Expected |
Mouse | Tested | Tested | Not recommended | Tested | Not recommended | Not recommended | Expected |
Rat | Tested | Tested | Not recommended | Tested | Not recommended | Not recommended | Expected |
Synthetic peptide - Human | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide - Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Mouse | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Rat | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide - Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat, Human, Synthetic peptide - Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide - Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Human, Rat, Synthetic peptide - Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat, Synthetic peptide - Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide - Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
ALDC, ALDOC, Fructose-bisphosphate aldolase C, Brain-type aldolase
Rabbit Recombinant Monoclonal Aldolase C antibody. Carrier free. Suitable for WB, IHC-P, ICC, I-ELISA and reacts with Human, Mouse, Rat, Synthetic peptide - Human samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Aldolase C also known as ALDOC is an enzyme that plays an important role in glycolysis. It catalyzes the reversible conversion of fructose-16-bisphosphate into dihydroxyacetone phosphate and glyceraldehyde-3-phosphate. Aldolase C has a molecular mass of approximately 39 kDa. This enzyme is primarily expressed in the brain particularly in astrocytes where it serves as an identifier for these cells.
This enzyme contributes to energy metabolism within cells notably astrocytes. It is part of the aldolase family which includes isoenzymes like aldolase A and B that perform similar functions in different tissues. Aldolase C is involved in maintaining glucose homeostasis and energy production in the brain where it forms part of a complex with other glycolytic enzymes to facilitate efficient cellular respiration.
Aldolase C is a significant component of the glycolytic pathway facilitating energy production in cells. It plays alongside other glycolytic enzymes such as hexokinase phosphofructokinase and pyruvate kinase to convert glucose into pyruvate transferring energy in the process. Additionally aldolase C participates in the fructose metabolism pathway similar to its isoenzymes aiding in the conversion of fructose derivatives important for maintaining normal energy levels in brain tissues.
Aldolase C has connections to neurological conditions like glioma and neurodegenerative diseases. Altered expression levels of aldolase C can indicate glioma progression or serve as a biomarker in astrocytic neurodegenerative disorders. The enzyme’s function is also linked to its interaction with other proteins such as Glial Fibrillary Acidic Protein (GFAP) in astrocytes which assist in maintaining normal cell structure and response to damage. Therefore aldolase C serves both as a metabolic enzyme and a potential marker in assessing neurological health and disease.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of 4% paraformaldehyde-fixed 0.1% TritonX-100 permeabilized mouse primary neuron/glial clells staining aldolase C with Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952 at 1/100 dilution adn secondary Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution. Counterstaining was done using ab10062 Anti-GFAP mouse monoclonal antibody at 1/50 dilution and secondary counterstain was Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) at 1/1000 dilution. Nucelar counterstain was DAPI (blue). Confocal image showing cytoplasmic staining in mouse primary neuron/glial. Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8).
Immunocytochemistry analysis of 4% paraformaldehyde-fixed 0.1% TritonX-100 permeabilized rat primary neuron/glial clells staining aldolase C with Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952 at 1/100 dilution and secondary Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution. Counterstaining was done using ab10062 Anti-GFAP mouse monoclonal antibody at 1/50 dilution and secondary counterstain was Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) at 1/1000 dilution. Nucelar counterstain was DAPI (blue). Confocal image showing cytoplasmic staining in rat primary neuron/glial. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
This data was developed using Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952, the same antibody clone in a different buffer formulation.
This data was developed using Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952, the same antibody clone in a different buffer formulation.
Indirect ELISA analysis of human Fructose-bisphosphate aldolase C N-terminal at 1000 ng/ml with ab30259 at concentration range 1000 - 0 ng/mL. An alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1/2500 dilution was used as the secondary antibody.
This data was developed using Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Exposure time: 5.5 seconds
Negative control: Pancreas (PMID: 31450822, 3513998)
Low expression: Heart (PMID: 3513998)
All lanes: Western blot - Anti-Aldolase C - N-terminal antibody [EPR26895-52] (Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952) at 1/1000 dilution
Lane 1: Mouse brain tissue lysate at 20 µg
Lane 2: Mouse cerebellum tissue lysate at 20 µg
Lane 3: Mouse pancreas tissue lysate at 20 µg
Lane 4: Mouse heart tissue lysate at 20 µg
Lane 5: Rat brain tissue lysate at 20 µg
Lane 6: Rat cerebellum tissue lysate at 20 µg
Lane 7: Rat pancreas tissue lysate at 20 µg
Lane 8: Rat heart tissue lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Predicted band size: 39 kDa
Observed band size: 39 kDa
Exposure time: 5.5s
This data was developed using Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Negative control: pancreas (PMID: 31450822, 3513998).
Low expression: heart (PMID:3513998).
All lanes: Western blot - Anti-Aldolase C - N-terminal antibody [EPR26895-52] (Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952) at 1/1000 dilution
Lane 1: Human heart tissue lysate at 20 µg
Lane 2: Human cerebellum tissue lysate at 20 µg
Lane 3: Human pancreas tissue lysate at 20 µg
Lane 4: U-87 MG (human glioblastoma-astrocytoma epithelial cell) whole cell lysate at 20 µg
Lane 5: RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate at 20 µg
Lane 6: C6 (rat glial tumor glial cell) whole cell lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Predicted band size: 39 kDa
Observed band size: 39 kDa
Exposure time: 70s
This data was developed using Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Exposure time: 5.5 seconds
This antibody does not cross-react with human ALDOA or ALDOB.
All lanes: Western blot - Anti-Aldolase C - N-terminal antibody [EPR26895-52] (Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952) at 1/1000 dilution
Lane 1: HEK-293T cells transfected with a Human ALDOC expression vector containi a myc-his tag, whole cell lysate at 20 µg
Lane 2: HEK-293T cells transfected with a Human ALDOA expression vector containing a myc-his tag, whole cell lysate at 20 µg
Lane 3: HEK-293T cells transfected with a Human ALDOB expression vector containi a myc-his tag, whole cell lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Predicted band size: 39 kDa
Observed band size: 39 kDa
Exposure time: 5.5s
This data was developed using Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat cerebrum tissue labeling Aldolase C N-terminal with Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952 at 1/5000 dilution (0.09 µg/ml), followed by a ready to use Leica DS9800 (Bond™ Polymer Refine Detection). Positive staining on rat cerebrum is observed. The section was incubated with Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use Leica DS9800 (Bond™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope retrieval solution 2) for 20 mins.
This data was developed using Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse cerebrum tissue labeling Aldolase C N-terminal with Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952 at 1/5000 dilution (0.09 µg/ml), followed by a ready to use Leica DS9800 (Bond™ Polymer Refine Detection). Positive staining on mouse cerebrum is observed. The section was incubated with Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use Leica DS9800 (Bond™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope retrieval solution 2) for 20 mins.
This data was developed using Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human pancreas tissue labeling Aldolase C N-terminal with Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952 at 1/2000 dilution (0.225 µg/ml), followed by a ready to use Leica DS9800 (Bond™ Polymer Refine Detection). Negative control: No staining is observed on human pancreas. The section was incubated with Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use Leica DS9800 (Bond™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope retrieval solution 2) for 20 mins.
This data was developed using Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human cerebrum tissue labeling Aldolase C N-terminal with Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952 at 1/2000 dilution (0.225 µg/ml) followed by a ready to use Leica DS9800 (Bond™ Polymer Refine Detection). Positive staining on human cerebrum is observed. The section was incubated with Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use Leica DS9800 (Bond™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope retrieval solution 2) for 20 mins.
This data was developed using Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded:
(A) HEK-293T cells transfected with a human ALDOC expression vector containing a myc-His tag
(B) HEK-293T cells transfected with a human ALDOA expression vector containing a myc-His tag
(C) HEK-293T cells transfected with a human ALDOB expression vector containing a myc-His tag
(D) HEK-293T cells transfected with empty vector containing a his tag
labeling Aldolase C N-terminal with Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952 at 1/5000 dilution (0.09 µg/ml), followed by a ready to use Leica DS9800 (Bond™ Polymer Refine Detection). Positive staining on (A) HEK-293T transfected with a ALDOC expression vector containing a myc-His tag, no staining on: (B) HEK-293T transfected with a ALDOA expression vector containing a myc-His tag, (C) HEK-293T transfected with a ALDOB expression vector containing a myc-His tag, and (D) HEK-293T transfected with empty plasmid. The section was incubated with Anti-Aldolase C - N-terminal antibody [EPR26895-52] ab302952 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use Leica DS9800 (Bond™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope retrieval solution 2) for 20 mins.
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