Anti-Aldolase C antibody [EPR26896-61] - C-terminal
- BOND RX™ Validated
- Recombinant
- 20ul selling size
- RabMAb
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Rabbit Recombinant Monoclonal Aldolase C antibody. Suitable for WB, I-ELISA, IHC-P and reacts with Human, Mouse, Synthetic peptide - Human samples.
View Alternative Names
ALDC, ALDOC, Fructose-bisphosphate aldolase C, Brain-type aldolase
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling Aldolase C - C-terminal with ab323506 at 1/10000 (0.049 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression tissue : No staining on human colon.
The section was incubated with ab323506 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Immunohistochemical analysis of paraffin-embedded Human cerebellum tissue labeling Aldolase C - C-terminal with ab323506 at 1/10000 (0.049 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human cerebellum.
The section was incubated with ab323506 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labeling Aldolase C - C-terminal with ab323506 at 1/10000 (0.049 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on astrocytes of human cerebrum.
The section was incubated with ab323506 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Immunohistochemical analysis of paraffin-embedded Human pancreas tissue labeling Aldolase C - C-terminal with ab323506 at 1/10000 (0.049 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression tissue : No staining on human pancreas.
The section was incubated with ab323506 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Immunohistochemical analysis of paraffin-embedded Mouse colon tissue labeling Aldolase C - C-terminal with ab323506 at 1/10000 (0.049 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression tissue : No staining on mouse colon.
The section was incubated with ab323506 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Immunohistochemical analysis of paraffin-embedded Mouse cardiac muscle tissue labeling Aldolase C - C-terminal with ab323506 at 1/10000 (0.049 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression tissue : No staining on mouse cardiac muscle.
The section was incubated with ab323506 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling Aldolase C - C-terminal with ab323506 at 1/10000 (0.049 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on astrocytes of mouse cerebrum.
The section was incubated with ab323506 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Immunohistochemical analysis of paraffin-embedded Mouse cerebellum tissue labeling Aldolase C - C-terminal with ab323506 at 1/10000 (0.049 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse cerebellum.
The section was incubated with ab323506 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- WB
Supplier Data
Western blot - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : pancreas, colon.
In Western blot, Anti-Histone H3 antibody [EPR16987] - Nuclear Marker and ChIP Grade (ab176842) staining at 1/100000 dilution.
All lanes:
Western blot - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (ab323506) at 1/1000 dilution
Lane 1:
Human cerebellum tissue lysate at 20 µg with NFDM/TBST
Lane 2:
Human pancreas tissue lysate at 20 µg with NFDM/TBST
Lane 3:
Human colon tissue lysate at 20 µg with NFDM/TBST
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 39 kDa,15 kDa
false
Exposure time: 1s
- WB
Supplier Data
Western blot - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (ab323506) at 1/1000 dilution
Lane 1:
Human brainstem tissue lysate at 20 µg with NFDM/TBST
Lane 2:
Human hippocampus tissue lysate at 20 µg with NFDM/TBST
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 39 kDa
false
Exposure time: 1s
- WB
Supplier Data
Western blot - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : Calu-3.
The identity of the bands higher than 50 kDa are unknown.
In Western blot, Anti-Histone H3 antibody [EPR16987] - Nuclear Marker and ChIP Grade (ab176842) staining at 1/100000 dilution.
All lanes:
Western blot - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (ab323506) at 1/1000 dilution
Lane 1:
U-87 MG (human glioblastoma-astrocytoma epithelial cell) whole cell lysate at 20 µg with NFDM/TBST
Lane 2:
LNCaP (human prostate carcinoma epithelial cell) whole cell lysate at 20 µg with NFDM/TBST
Lane 3:
Calu-3 (human lung adenocarcinoma epithelial cell) whole cell lysate at 20 µg with NFDM/TBST
Lane 4:
RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate at 20 µg with NFDM/TBST
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 39 kDa,15 kDa
false
Exposure time: 8s
- WB
Supplier Data
Western blot - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : pancreas.
In Western blot, Anti-Histone H3 antibody [EPR16987] - Nuclear Marker and ChIP Grade (ab176842) staining at 1/100000 dilution.
All lanes:
Western blot - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (ab323506) at 1/1000 dilution
Lane 1:
Mouse cerebellum tissue lysate at 20 µg with NFDM/TBST
Lane 2:
Mouse brain tissue lysate at 20 µg with NFDM/TBST
Lane 3:
Mouse pancreas tissue lysate at 20 µg with NFDM/TBST
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 39 kDa,15 kDa
false
Exposure time: 1s
- I-ELISA
Supplier Data
Indirect ELISA - Anti-Aldolase C antibody [EPR26896-61] - C-terminal (AB323506)
Indirect ELISA analysis of ab323506 at 1000-0 ng/ml. The Secondary antibody used was Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1 : 2500 dilution dilution.
Antigen : Human ALDOC peptide, Human ALDOA peptide, Human ALDOB peptide.
Antigen concentration : 1000 ng/ml
This antibody does not cross-react with human ALDOA and ALDOB
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
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.
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