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AB307370

Anti-OGDH antibody [EPR27181-78] - BSA and Azide free

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(1 Publication)

Rabbit Recombinant Monoclonal OGDH antibody. Carrier free. Suitable for Flow Cyt (Intra), ICC/IF, IHC-Fr, IHC-P, WB and reacts with Mouse, Human, Rat, Transfected cell lysate - Human samples. Cited in 1 publication.

View Alternative Names

2-oxoglutarate dehydrogenase complex component E1, E1o, HsOGDH, OGDC-E1, OGDH-E1, Alpha-ketoglutarate dehydrogenase, Thiamine diphosphate (ThDP)-dependent 2-oxoglutarate dehydrogenase, Alpha-KGDH-E1, OGDH

17 Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using ab307369, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human cardiac muscle tissue lABeling OGDH with ab307369 at 1/2000 (0.232 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Cytoplasmic staining on human cardiac muscle (PMID : 31682939). The section was incubated with ab307369 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 LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using ab307369, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human kidney tissue lABeling OGDH with ab307369 at 1/2000 (0.232 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Cytoplasmic staining on human kidney. The section was incubated with ab307369 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 LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

Immunocytochemistry/ Immunofluorescence - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • ICC/IF

Supplier Data

Immunocytochemistry/ Immunofluorescence - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using ab307369, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeABilized HeLa (human cervical adenocarcinoma epithelial cell) cells lABelling OGDH with ab307369 at 1/100 (4.64 ug/ml) dilution, followed by ab150081 Goat Anti-RABbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing mitochondrial staining in HeLa cell line. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). is observed. ab33985 Anti-COX IV mouse monoclonal antibody - Mitochondrial Marker was used to counterstain tubulin at 1/1000 1ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-RABbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.

Flow Cytometry (Intracellular) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • Flow Cyt (Intra)

Supplier Data

Flow Cytometry (Intracellular) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using ab307369, the same antibody clone in a different buffer formulation.

Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized HeLa (human cervix adenocarcinoma epithelial cell) cells labelling OGDH with ab307369 at 1/50 dilution (1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.

Immunohistochemistry (Frozen sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • IHC-Fr

Supplier Data

Immunohistochemistry (Frozen sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using ab307369, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse spleen (fresh) tissue labeling OGDH with ab307369 at 1/50 (9.28 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Low expression : confocal image showing no staining on mouse spleen (PMID : 35540547). The nuclear counterstain was DAPI (Blue). The section was incubated with ab307369 for 60 mins at room temperature. The section was then mounted using Fluoromount®. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution.

Immunohistochemistry (Frozen sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • IHC-Fr

Supplier Data

Immunohistochemistry (Frozen sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using ab307369, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse kidney (fresh) tissue labeling OGDH with ab307369 at 1/50 (9.28 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Confocal image showing positive staining on mouse kidney. The nuclear counterstain was DAPI (Blue). The section was incubated with ab307369 for 60 mins at room temperature. The section was then mounted using Fluoromount®. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution.

Immunocytochemistry/ Immunofluorescence - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • ICC/IF

Supplier Data

Immunocytochemistry/ Immunofluorescence - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using ab307369, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeABilized NIH/3T3 (mouse embryonic fibroblast) cells lABelling OGDH with ab307369 at 1/100 (4.64 ug/ml) dilution, followed by ab150081 Goat Anti-RABbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing mitochondrial staining in NIH/3T3 cell line. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-RABbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using ab307369, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded rat kidney tissue labeling OGDH with ab307369 at 1/2000 dilution (0.232 μg/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Cytoplasmic staining on rat kidney.
The section was incubated with ab307369 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 ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using ab307369, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat cardiac muscle tissue labeling OGDH with ab307369 at 1/2000 (0.232 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Cytoplasmic staining on rat cardiac muscle (PMID : 31682939). The section was incubated with ab307369 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 LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using ab307369, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded mouse kidney tissue labeling OGDH with ab307369 at 1/2000 dilution (0.232 μg/ml) followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Cytoplasmic staining on mouse kidney.
The section was incubated with ab307369 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 ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • IHC-P

Supplier Data

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using ab307369, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse cardiac muscle tissue labeling OGDH with ab307369 at 1/2000 (0.232 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Cytoplasmic staining on mouse cardiac muscle (PMID : 31682939). The section was incubated with ab307369 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 LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

Flow Cytometry (Intracellular) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • Flow Cyt (Intra)

Supplier Data

Flow Cytometry (Intracellular) - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using ab307369, the same antibody clone in a different buffer formulation.

Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized NIH/3T3 (mouse embryonic fibroblast) cells labelling OGDH with ab307369 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.

Western blot - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • WB

Supplier Data

Western blot - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using 307369, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 3 seconds Exposure time :

All lanes:

Western blot - Anti-OGDH antibody [EPR27181-78] (<a href='/en-us/products/primary-antibodies/ogdh-antibody-epr27181-78-ab307369'>ab307369</a>) at 1/1000 dilution

Lane 1:

Human heart tissue lysate 20 μg

Lane 2:

Human kidney tissue lysate 20 μg

Secondary

All lanes:

Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution

Observed band size: 116 kDa

false

Exposure time: 3s

Western blot - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • WB

Supplier Data

Western blot - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using 307369, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : The identity of the lower MW band at approximately 40 kDa is unknown. 180 seconds Exposure time :

All lanes:

Western blot - Anti-OGDH antibody [EPR27181-78] (<a href='/en-us/products/primary-antibodies/ogdh-antibody-epr27181-78-ab307369'>ab307369</a>) at 1/1000 dilution

Lane 1:

HeLa (human cervical adenocarcinoma epithelial cell) transfected with scrambled siRNA control whole cell lysate 20 μg

Lane 2:

HeLa transfected with siRNA specifically targeti OGDH whole cell lysate 20 μg

Lane 3:

293T (human embryonic kidney epithelial cell) whole cell lysate 20 μg

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 1/100000 dilution

Observed band size: 116 kDa

false

Exposure time: 180s

Western blot - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • WB

Supplier Data

Western blot - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using 307369, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 180 seconds Exposure time :

All lanes:

Western blot - Anti-OGDH antibody [EPR27181-78] (<a href='/en-us/products/primary-antibodies/ogdh-antibody-epr27181-78-ab307369'>ab307369</a>) at 1/1000 dilution

Lane 1:

C6 (rat glial tumor glial cell) whole cell lysate 20 μg

Lane 2:

RAW 264.7 (mouse elson murine leukemia virus-induced tumor macrophage) whole cell lysate 20 μg

Lane 3:

PC-12 (rat adrenal gland pheochromocytoma cell) whole cell lysate 20 μg

Lane 4:

NIH/3T3 (mouse embryonic fibroblast) whole cell lysate 20 μg

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 1/100000 dilution

Observed band size: 116 kDa

false

Exposure time: 180s

Western blot - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • WB

Supplier Data

Western blot - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using 307369, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : Low expression tissue : spleen (PMID : 35540547). 15 seconds Exposure time :

All lanes:

Western blot - Anti-OGDH antibody [EPR27181-78] (<a href='/en-us/products/primary-antibodies/ogdh-antibody-epr27181-78-ab307369'>ab307369</a>) at 1/1000 dilution

Lane 1:

Mouse heart tissue lysate 20 μg

Lane 2:

Mouse kidney tissue lysate 20 μg

Lane 3:

Mouse spleen tissue lysate 20 μg

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 1/100000 dilution

Observed band size: 116 kDa

false

Exposure time: 15s

Western blot - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)
  • WB

Supplier Data

Western blot - Anti-OGDH antibody [EPR27181-78] - BSA and Azide free (AB307370)

This data was developed using 307369, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : Low expression tissue : spleen (PMID : 35540547). 10 seconds Exposure time :

All lanes:

Western blot - Anti-OGDH antibody [EPR27181-78] (<a href='/en-us/products/primary-antibodies/ogdh-antibody-epr27181-78-ab307369'>ab307369</a>) at 1/1000 dilution

Lane 1:

Rat heart tissue lysate 20 μg

Lane 2:

Rat kidney tissue lysate 20 μg

Lane 3:

Rat spleen tissue lysate 20 μg

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 1/100000 dilution

Observed band size: 116 kDa

false

Exposure time: 10s

Key facts

Host species

Rabbit

Clonality

Monoclonal

Clone number

EPR27181-78

Isotype

IgG

Carrier free

Yes

Reacts with

Rat, Mouse, Human

Applications

ICC/IF, IHC-P, Flow Cyt (Intra), IHC-Fr, WB

applications

Immunogen

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

Reactivity data

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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.

Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. 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.

Compatibility
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.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein A
Storage buffer
pH: 7.2 - 7.4 Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C

Supplementary information

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

OGDH also known as alpha-ketoglutarate dehydrogenase or a-ketoglutarate dehydrogenase is an enzyme that plays a significant role in metabolism. It catalyzes the conversion of alpha-ketoglutarate into succinyl-CoA and CO2 in the tricarboxylic acid (TCA) cycle also known as the Krebs cycle. The enzyme functions as a part of a multi-enzyme complex and has a molecular mass of approximately 1 MDa. OGDH is expressed in various tissues with higher levels typically found in the mitochondria of cells reflecting its role in cellular respiration.
Biological function summary

OGDH is critical for energy production by enabling the TCA cycle to proceed. It is a component of the alpha-ketoglutarate dehydrogenase complex consisting of multiple subunits which include E1 (OGDH itself) E2 (dihydrolipoamide succinyltransferase) and E3 (dihydrolipoamide dehydrogenase). This complex functions to ensure the proper oxidation of metabolites important for maintaining cellular energy homeostasis. Proper regulation of OGDH activity impacts several metabolic pathways influencing cellular glucose and lipid metabolism.

Pathways

OGDH is integrally involved in the TCA cycle a central metabolic pathway that connects carbohydrate fat and protein metabolism. Alongside related enzymes like pyruvate dehydrogenase (PDH) and isocitrate dehydrogenase (IDH) OGDH contributes to the generation of NADH and FADH2 essential carriers in the electron transport chain. The interplay between these enzymes ensures the smooth functioning of aerobic respiration linking glycolysis and oxidative phosphorylation.

OGDH has links to neurodegenerative diseases such as Alzheimer's and Parkinson's disease. Abnormal activity of OGDH can lead to mitochondrial dysfunction a common feature observed in these disorders. The protein connects to pathways involving PDH dysfunction contributing to altered metabolic states seen in these conditions. Research continues to explore the potential of targeting OGDH in therapeutic strategies aimed at improving mitochondrial health and energy metabolism in affected patients.

Product protocols

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

Target data

2-oxoglutarate dehydrogenase (E1o) component of the 2-oxoglutarate dehydrogenase complex (OGDHC) (PubMed : 24495017, PubMed : 25210035, PubMed : 28435050). Participates in the first step, rate limiting for the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2) catalyzed by the whole OGDHC (PubMed : 24495017, PubMed : 25210035, PubMed : 28435050). Catalyzes the irreversible decarboxylation of 2-oxoglutarate (alpha-ketoglutarate) via the thiamine diphosphate (ThDP) cofactor and subsequent transfer of the decarboxylated acyl intermediate on an oxidized dihydrolipoyl group that is covalently amidated to the E2 enzyme (dihydrolipoyllysine-residue succinyltransferase or DLST) (PubMed : 24495017, PubMed : 25210035, PubMed : 28435050, PubMed : 35272141). Plays a key role in the Krebs (citric acid) cycle, which is a common pathway for oxidation of fuel molecules, including carbohydrates, fatty acids, and amino acids (PubMed : 25210035). Can catalyze the decarboxylation of 2-oxoadipate in vitro, but at a much lower rate than 2-oxoglutarate (PubMed : 28435050). Can also convert 2-keto-4-hydroxyglutarate (KHG) and CoA into malyl-CoA (By similarity). Mainly active in the mitochondrion (PubMed : 29211711). A fraction of the 2-oxoglutarate dehydrogenase complex also localizes in the nucleus and is required for lysine succinylation of histones : associates with KAT2A on chromatin and provides succinyl-CoA to histone succinyltransferase KAT2A (PubMed : 29211711).
See full target information 2-oxoglutarate dehydrogenase, mitochondrial

Publications (1)

Recent publications for all applications. Explore the full list and refine your search

NPJ Regenerative medicine 9:43 PubMed39738050

2024

Macrophage-derived extracellular vesicles transfer mitochondria to adipocytes and promote adipocyte-myofibroblast transition in epidural fibrosis.

Applications

Unspecified application

Species

Unspecified reactive species

Feng Hua,Jinpeng Sun,Mohan Shi,Rui Mei,Zeyuan Song,Jun Liu,Mingshun Zhang
View all publications

Product promise

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