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Merck
CN

MABN457

Sigma-Aldrich

Anti-Mitochondrial dicarboxylate carrier Antibody, clone 1F5.1

clone 1F5.1, from mouse

Synonym(s):

Mitochondrial dicarboxylate carrier, Solute carrier family 25 member 10

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
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biological source

mouse

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

1F5.1, monoclonal

species reactivity

rat, mouse

technique(s)

immunohistochemistry: suitable
western blot: suitable

isotype

IgG1κ

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

mouse ... Slc25A10(27376)

General description

The protein named Mitochondrial dicarboxylate carrier or Solute carrier family 25 member 10, or Dicarboxylate Carrier Slc25a10 and encoded by the gene named SLC25A10 or DIC is a mitochondrial transport protein that mediates the transfer of malonate, malate, and succinate in exchange for phosphate, sulfate, sulfite or thiosulfate across the mitochondrial inner membrane. These components are critical for the function of the Krebs cycle, as well as gluconeogenesis, urea and sulfur metabolism. Mitochondrial dicarboxylate carrier is expressed in high amounts in the liver and kidney and at lower levels in all other tissues and is localized to the mitochondria and specifically to the inner mitochondrial membrane. Mitochondrial dicarboxylate carrier is also upregulated in various tissues in response to free fatty acids particularly in adipose tissues, and plays a role in mitochondrial malate transport and in the regulation of glucose-stimulated insulin secretion from pancreatic beta cells. Impairment of Mitochondrial dicarboxylate carrier is associated with ethylmalonic encephalopathy (EE) and short chain acyl-CoA dehydrogenase deficiency (SCADD) syndromes. Research indicates that it is the buildup of ethylmalonic acid in the tissues that impairs the Succinate and malate uptake by Mitochondrial dicarboxylate carrier leading to metabolic distress and dysfunction.
~32 kDa observed

Immunogen

KLH-conjugated linear peptide corresponding to human Mitochondrial dicarboxylate carrier.

Application

Anti-Mitochondrial dicarboxylate carrier Antibody, clone 1F5.1 is a highly specific mouse monoclonal antibody, that targets Solute carrier family 25 member 10 & has been tested in western blotting & IHC.
Immunohistochemistry Analysis: A 1:500 dilution from a representative lot detected Mitochondrial dicarboxylate carrier in human kidney and human liver tissue.
Research Category
Neuroscience
Research Sub Category
Developmental Signaling

Physical form

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG1κ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Preparation Note

Stable for 1 year at 2-8°C from date of receipt.

Analysis Note

Evaluated by Western Blotting in mouse liver tissue lysate.

Western Blotting Analysis: 1.0 µg/mL of this antibody detected Mitochondrial dicarboxylate carrier in 200 µg of mouse liver tissue lysate.

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sehwan Jang et al.
Redox biology, 45, 102021-102021 (2021-06-09)
Ferroptosis is a programmed iron-dependent cell death associated with peroxidation of lipids particularly, phospholipids. Several studies suggested a possible contribution of mitochondria to ferroptosis although the mechanisms underlying mitochondria-mediated ferroptotic pathways remain elusive. Reduced glutathione (GSH) is a central player

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