Date published: 2026-4-5

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citrin Antibody (D-7): sc-393303

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Datasheets
  • citrin Antibody (D-7) is a mouse monoclonal IgA κ citrin antibody, cited in 3 publications, provided at 200 µg/ml
  • specific for an epitope mapping between amino acids 30-51 near the N-terminus of citrin of human origin
  • recommended for detection of citrin of mouse, rat and human origin by WB, IP, IF, IHC(P) and ELISA; also reactive with additional species, including and canine, bovine and porcine
  • At present, we have not yet completed the identification of the preferred secondary detection reagent(s) for citrin Antibody (D-7). This work is in progress.
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Citrin Antibody (D-7) is a mouse monoclonal IgA kappa light chain antibody that detects citrin protein of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), immunohistochemistry, and enzyme-linked immunosorbent assay (ELISA). Anti-citrin antibody (D-7) is available as the non-conjugated form. Citrin, also known as SLC25A13 (Solute carrier family 25 member 13), ARALAR2, or CTLN2, is a 675 amino acid multi-pass membrane protein primarily localized to the inner membrane of the mitochondrion. This localization enables citrin to transport calcium-dependent glutamate and aspartate, playing a significant role in the urea cycle, which is essential for nitrogen metabolism and detoxification in the liver. Citrin protein is expressed in various tissues, including the liver, pancreas, kidney, brain, heart, and placenta, highlighting its importance in multiple physiological processes. Citrin features three Solcar repeats and four EF-hand domains that facilitate calcium binding as a member of the mitochondrial carrier family. Mutations in citrin can lead to serious metabolic disorders such as citrullinemia type 2 (CTLN2) and neonatal intrahepatic cholestasis due to citrin deficiency (NICCD). CTLN2 is an autosomal recessive condition characterized by neuropsychiatric symptoms, including memory loss, seizures, and coma, while NICCD manifests during infancy with symptoms such as low birth weight, reduced bile flow, growth retardation, and hepatic fibrosis.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences

citrin Antibody (D-7) References:

  1. The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein.  |  Kobayashi, K., et al. 1999. Nat Genet. 22: 159-63. PMID: 10369257
  2. Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13, and cloning and expression of its mouse homologue.  |  Sinasac, DS., et al. 1999. Genomics. 62: 289-92. PMID: 10610724
  3. Characterization of a second member of the subfamily of calcium-binding mitochondrial carriers expressed in human non-excitable tissues.  |  Del Arco, A., et al. 2000. Biochem J. 345 Pt 3: 725-32. PMID: 10642534
  4. Citrin and aralar1 are Ca(2+)-stimulated aspartate/glutamate transporters in mitochondria.  |  Palmieri, L., et al. 2001. EMBO J. 20: 5060-9. PMID: 11566871
  5. Screening of SLC25A13 mutations in early and late onset patients with citrin deficiency and in the Japanese population: Identification of two novel mutations and establishment of multiple DNA diagnosis methods for nine mutations.  |  Yamaguchi, N., et al. 2002. Hum Mutat. 19: 122-30. PMID: 11793471
  6. Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD).  |  Saheki, T. and Kobayashi, K. 2002. J Hum Genet. 47: 333-41. PMID: 12111366
  7. Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency.  |  Lu, YB., et al. 2005. J Hum Genet. 50: 338-346. PMID: 16059747
  8. Adult onset type II citrullinemia as a cause of non-alcoholic steatohepatitis.  |  Takagi, H., et al. 2006. J Hepatol. 44: 236-9. PMID: 16278034
  9. Downregulation of citrin, a mitochondrial AGC, is associated with apoptosis of hepatocytes.  |  Sawada, S., et al. 2007. Biochem Biophys Res Commun. 364: 937-44. PMID: 18273444

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

citrin Antibody (D-7)

sc-393303
200 µg/ml
$322.00

citrin (D-7) Neutralizing Peptide

sc-393303 P
100 µg/0.5 ml
$69.00

What application is the blocking peptide sc-393303 P appropriate for?

Asked by: TinTin
Thank you for your question. The blocking peptide is intended for use as a negative control, by pre-adsorbing the mouse monoclonal antibody against the antigen. For full protocol details, please contact our Technical Services Department or view our online protocol here: https://www.scbt.com/scbt/resources/protocols/peptide-neutralization
Answered by: Technical Support
Date published: 2017-02-24
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Rated 4 out of 5 by from good for WBit works well for WB in our lab, not a bad choice.
Date published: 2017-09-18
Rated 5 out of 5 by from Satisfactory Western Blot data of citrinSatisfactory Western Blot data of citrin expression in human liver tissue extract. -SCBT QC
Date published: 2015-04-13
Rated 5 out of 5 by from Great Western Blot data of citrin expressionGreat Western Blot data of citrin expression in Hep G2 whole cell lysate. -SCBT QC
Date published: 2013-04-03
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citrin Antibody (D-7) is rated 4.7 out of 5 by 3.
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