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Solute Carrier Family 25, Member 13 (Citrin) (slc25a13) ELISA Kits

slc25a13 is a member of the mitochondrial carrier family. Additionally we are shipping slc25a13 Antibodies (47) and slc25a13 Proteins (5) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
slc25a13 10165 Q9UJS0
Anti-Rat slc25a13 slc25a13 362322  
slc25a13 50799 Q9QXX4
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Top slc25a13 ELISA Kits at antibodies-online.com

Showing 2 out of 3 products:

Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Human 0.312-20 ng/mL 96 Tests Log in to see 11 to 13 Days
$875.60
Details
Mouse
96 Tests Log in to see 11 to 13 Days
$875.60
Details

More ELISA Kits for slc25a13 Interaction Partners

Human Solute Carrier Family 25, Member 13 (Citrin) (slc25a13) interaction partners

  1. This study aims to screen for five prevalent SLC25A13 mutations, to calculate the mutation carrier rate in Guangdong.

  2. we reviewed the English literature on mutations in the SLC25A13 gene, and its genotype-phenotype correlations to provide valuable insights into the molecular genetic background of citrullinemia (show ASS1 ELISA Kits)--{REVIEW}

  3. Mutation screening of the SLC25A13 gene revealed the compound heterozygous mutations c.1081C>T (p.R361*) and c.74C>A (p. A25E) which confirmed the diagnosis of NICCD. The nonsense mutation c.1081C>T (p.R361*) is novel.

  4. Point mutation of ASS1 (show ASS1 ELISA Kits), ASL (show ADSL ELISA Kits) and SLC25A13 is associated with citrullinemia (show ASS1 ELISA Kits).

  5. Identification of novel SLC25A13 gene mutations in East Asian patients with citrin deficiency.

  6. Analysis of the SLC25A13 gene sequence.

  7. Report frequency SLC25A13 mutations in the Thai population and estimate prevalence of citrin deficiency.

  8. The SLC25A13 mutation spectra among the three regions of China were different, providing a basis for the improvement of diagnostic strategies and interpretation of genetic diagnosis.

  9. Compares and contrasts all the known human SLC25A (show SLC25A25 ELISA Kits)* genes and includes functional information.

  10. The objectives were to study the prevalence of neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) in Thai infants with idiopathic cholestasis, mutation spectrum of SLC25A13 in Thai NICCD, and comparison of clinical manifestations and blood chemistry between NICCD and non-NICCD infants.

Mouse (Murine) Solute Carrier Family 25, Member 13 (Citrin) (slc25a13) interaction partners

  1. hepatic metabolite perturbations in citrin-mitochondrial glycerol-3-phosphate dehydrogenase (show GPD1 ELISA Kits) double-knockout mice, a model of human citrin deficiency

  2. The results support the notion that glial cells have much lower AGC (show ACAN ELISA Kits) levels and MAS (show MAS1 ELISA Kits) activity than neurons

  3. Expression of the aspartate/glutamate (show GRIN1 ELISA Kits) mitochondrial carriers aralar1 (show Slc25a12 ELISA Kits) and citrin during development(CITRIN)

  4. To investigate the physiological role of citrin and the development of CTLN2 (adult-onset type II citrullinemia (show ASS1 ELISA Kits)), an Slc25a13-knockout mouse model was created.

  5. Aralar and citrin, when expressed as single isoforms in heart, confer differences in Ca(2 (show CA2 ELISA Kits)+) activation of shuttle activity, probably associated with their structural differences.

  6. phenotypic analysis of citrin/mitochondrial glycerol-3-phosphate dehydrogenase (show GPD1 ELISA Kits) double knock-out mice

slc25a13 Antigen Profile

Antigen Summary

This gene is a member of the mitochondrial carrier family. The encoded protein contains four EF-hand Ca(2+) binding motifs in the N-terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with slc25a13

  • solute carrier family 25 (aspartate/glutamate carrier), member 13 (SLC25A13) antibody
  • solute carrier family 25, member 13 (citrin) (slc25a13) antibody
  • solute carrier family 25, member 13 (citrin) (SLC25A13) antibody
  • solute carrier family 25 (aspartate/glutamate carrier), member 12 (slc25a12) antibody
  • solute carrier family 25 (aspartate/glutamate carrier), member 13 (slc25a13) antibody
  • solute carrier family 25 (aspartate/glutamate carrier), member 13 (Slc25a13) antibody
  • solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 (Slc25a13) antibody
  • AI785475 antibody
  • aralar antibody
  • aralar1 antibody
  • ARALAR2 antibody
  • CITRIN antibody
  • CTLN2 antibody
  • Ctrn antibody
  • MGC69168 antibody
  • RGD1565889 antibody
  • slc25a13 antibody

Protein level used designations for slc25a13

solute carrier family 25, member 13 (citrin) , solute carrier family 25 (mitochondrial carrier, Aralar), member 12 , solute carrier family 25, member 12 , solute carrier family 25, member 13 , calcium-binding mitochondrial carrier protein Aralar2-like , calcium-binding mitochondrial carrier protein Aralar2 , mitochondrial aspartate glutamate carrier 2 , solute carrier family 25 (aspartate/glutamate carrier), member 13 tv2 , solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 , citrin , solute carrier family 25 member 13

GENE ID SPECIES
100063046 Equus caballus
398810 Xenopus laevis
472450 Pan troglodytes
549674 Xenopus (Silurana) tropicalis
699911 Macaca mulatta
100124779 Xenopus (Silurana) tropicalis
100401767 Callithrix jacchus
100434018 Pongo abelii
100466909 Ailuropoda melanoleuca
100561177 Anolis carolinensis
100606811 Nomascus leucogenys
10165 Homo sapiens
610138 Canis lupus familiaris
100524162 Sus scrofa
615470 Bos taurus
362322 Rattus norvegicus
50799 Mus musculus
428427 Gallus gallus
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