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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.

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Images

Immunocytochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (AB302953), expandable thumbnail
  • Immunocytochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (AB302953), expandable thumbnail
  • Indirect ELISA - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (AB302953), expandable thumbnail
  • Western blot - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (AB302953), expandable thumbnail
  • Western blot - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (AB302953), expandable thumbnail

Key facts

Isotype
IgG
Host species
Rabbit
Storage buffer

pH: 7.2 - 7.4
Constituents: 100% PBS

Form
Liquid
Clonality
Monoclonal

Immunogen

  • The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

Select an application
Product promiseTestedExpectedPredictedNot recommended
WBIHC-PIHC-FrICCFlow Cyt (Intra)IPI-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

Tested
Tested

Species
Human, Mouse, Rat
Dilution info
-
Notes

-

Not recommended
Not recommended

Species
Synthetic peptide - Human
Dilution info
-
Notes

-

Tested
Tested

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.

Not recommended
Not recommended

Species
Synthetic peptide - Human
Dilution info
-
Notes

-

Not recommended
Not recommended

Species
Mouse, Rat, Human, Synthetic peptide - Human
Dilution info
-
Notes

-

Tested
Tested

Species
Mouse, Rat
Dilution info
-
Notes

-

Expected
Expected

Species
Human
Dilution info
Use at an assay dependent concentration.
Notes

-

Not recommended
Not recommended

Species
Synthetic peptide - Human
Dilution info
-
Notes

-

Not recommended
Not recommended

Species
Mouse, Human, Rat, Synthetic peptide - Human
Dilution info
-
Notes

-

Not recommended
Not recommended

Species
Human, Mouse, Rat, Synthetic peptide - Human
Dilution info
-
Notes

-

Tested
Tested

Species
Synthetic peptide - Human
Dilution info
-
Notes

-

Expected
Expected

Species
Human, Mouse, Rat
Dilution info
Use at an assay dependent concentration.
Notes

-

Alternative names

Recommended products

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.

Key facts

Isotype
IgG
Form
Liquid
Clonality
Monoclonal
Immunogen
  • The exact immunogen used to generate this antibody is proprietary information.
Carrier free
Yes
Clone number
EPR26895-52
Purification technique
Affinity purification Protein A
Concentration
Loading...

Storage

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C

Notes

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:

  • - High batch-to-batch consistency and reproducibility
  • - Improved sensitivity and specificity
  • - Long-term security of supply
  • - Animal-free batch production

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.

Supplementary info

This supplementary information is collated from multiple sources and compiled automatically.
Activity summary

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.

Biological function summary

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.

Pathways

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.

Associated diseases and disorders

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.

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.

11 product images

  • Immunocytochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953), expandable thumbnail

    Immunocytochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953)

    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 - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953), expandable thumbnail

    Immunocytochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953)

    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.

  • Indirect ELISA - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953), expandable thumbnail

    Indirect ELISA - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953)

    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.

  • Western blot - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953), expandable thumbnail

    Western blot - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953)

    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

    Secondary

    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

  • Western blot - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953), expandable thumbnail

    Western blot - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953)

    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

    Secondary

    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

  • Western blot - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953), expandable thumbnail

    Western blot - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953)

    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

    Secondary

    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

  • Immunohistochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953), expandable thumbnail

    Immunohistochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953)

    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. 

  • Immunohistochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953), expandable thumbnail

    Immunohistochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953)

    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. 

  • Immunohistochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953), expandable thumbnail

    Immunohistochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953)

    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. 

  • Immunohistochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953), expandable thumbnail

    Immunohistochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953)

    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. 

  • Immunohistochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953), expandable thumbnail

    Immunohistochemistry - Anti-Aldolase C - N-terminal antibody [EPR26895-52] - BSA and Azide free (ab302953)

    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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Product protocols

For this product, it's our understanding that no specific protocols are required. You can:

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