Anti-SLC25A13 Antibody (CAB5849)

Antibody Name:	Anti-SLC25A13 Antibody
Antibody SKU:	CAB5849
Antibody Size:	20uL, 50uL, 100uL
Application:	WB IHC
Reactivity:	Human, Mouse
Host Species:	Rabbit
Immunogen:	Recombinant fusion protein containing a sequence corresponding to amino acids 1-300 of human SLC25A13 (NP_001153682.1).

Application:	WB IHC
Recommended Dilution:	WB 1:500 - 1:2000 IHC 1:50 - 1:200
Reactivity:	Human, Mouse
Positive Samples:	MCF7, SW480, 293T, HepG2, HeLa, Mouse liver, Mouse kidney

Immunogen:	Recombinant fusion protein containing a sequence corresponding to amino acids 1-300 of human SLC25A13 (NP_001153682.1).
Purification Method:	Affinity purification
Storage Buffer:	Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Isotype:	IgG
Sequence:	MAAA KVAL TKRA DPAE LRTI FLKY ASIE KNGE FFMS PNDF VTRY LNIF GESQ PNPK TVEL LSGV VDQT KDGL ISFQ EFVA FESV LCAP DALF MVAF QLFD KAGK GEVT FEDV KQVF GQTT IHQH IPFN WDSE FVQL HFGK ERKR HLTY AEFT QFLL EIQL EHAK QAFV QRDN ARTG RVTA IDFR DIMV TIRP HVLT PFVE ECLV AAAG GTTS HQVS FSYF NGFN SLLN NMEL IRKI YSTL AGTR KDVE VTKE EFVL AAQK FGQV TPME VDIL FQLA DLYE PRGR MTLA DIER IAPL EEGT
Gene ID:	10165
Uniprot:	Q9UJS0
Cellular Location:	Mitochondrion inner membrane, Multi-pass membrane protein
Calculated MW:	74kDa
Observed MW:	73kDa

Synonyms:

SLC25A13, ARALAR2, CITRIN, CTLN2

Background:

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.

UniProt Protein Function:	SLC25A13: Catalyzes the calcium-dependent exchange of cytoplasmic glutamate with mitochondrial aspartate across the mitochondrial inner membrane. May have a function in the urea cycle. Defects in SLC25A13 are the cause of citrullinemia type 2 (CTLN2). Citrullinemia belongs to the urea cycle disorders. It is an autosomal recessive disease characterized primarily by elevated serum and urine citrulline levels. Ammonia intoxication is another manifestation. CTLN2 is characterized by neuropsychiatric symptoms including abnormal behaviors, loss of memory, seizures and coma. Death can result from brain edema. Onset is sudden and usually between the ages of 20 and 50 years. Defects in SLC25A13 are the cause of neonatal intrahepatic cholestasis due to citrin deficiency (NICCD). NICCD is a form of citrullinemia type 2 with neonatal onset. NICCD is characterized by suppression of the bile flow, hepatic fibrosis, low birth weight, growth retardation, hypoproteinemia, variable liver dysfunction. NICCD is generally not severe and symptoms disappear by one year of age with an appropriate diet. Years or even decades later, however, some individuals develop the characteristic features of citrullinemia type 2 with neuropsychiatric symptoms. Belongs to the mitochondrial carrier family. 2 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:	Protein type:Mitochondrial; Membrane protein, multi-pass; Membrane protein, integral; Transporter, SLC family; Transporter Chromosomal Location of Human Ortholog: 7q21.3 Cellular Component: mitochondrion; integral to plasma membrane; mitochondrial inner membrane Molecular Function:L-aspartate transmembrane transporter activity; transporter activity; calcium ion binding; L-glutamate transmembrane transporter activity Biological Process: L-glutamate transport; transport; ATP biosynthetic process; carbohydrate metabolic process; cellular respiration; glucose metabolic process; pathogenesis; aspartate transport; malate-aspartate shuttle; response to calcium ion; gluconeogenesis Disease: Citrullinemia, Type Ii, Adult-onset; Citrullinemia, Type Ii, Neonatal-onset
NCBI 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. [provided by RefSeq, May 2009]
UniProt Code:	Q9UJS0
NCBI GenInfo Identifier:	13124095
NCBI Gene ID:	10165
NCBI Accession:	Q9UJS0.2
UniProt Related Accession:	Q9UJS0
Molecular Weight:
NCBI Full Name:	Calcium-binding mitochondrial carrier protein Aralar2
NCBI Synonym Full Names:	solute carrier family 25 member 13
NCBI Official Symbol:	SLC25A13
NCBI Official Synonym Symbols:	CTLN2; CITRIN; ARALAR2
NCBI Protein Information:	calcium-binding mitochondrial carrier protein Aralar2
UniProt Protein Name:	Calcium-binding mitochondrial carrier protein Aralar2
UniProt Synonym Protein Names:	Citrin; Mitochondrial aspartate glutamate carrier 2; Solute carrier family 25 member 13
Protein Family:	COX assembly mitochondrial protein
UniProt Gene Name:	SLC25A13
UniProt Entry Name:	CMC2_HUMAN

	Western blot analysis of extracts of various cell lines, using SLC25A13 antibody (CAB5849) at 1:1000 dilution._Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution._Lysates/proteins: 25ug per lane._Blocking buffer: 3% nonfat dry milk in TBST._Detection: ECL Basic Kit (RM00020)._Exposure time: 90s.
	Immunohistochemistry of paraffin-embedded mouse heart using SLC25A13 antibody (CAB5849) at dilution of 1:200 (40x lens).

Antibodies	ELISA Kits
Anti-SLC25A13 Antibody (CAB12557)	Human SLC25A13 / Aralar2 ELISA Kit
SLC25A13 Antibody (PACO12261)	Human Calcium-binding mitochondrial carrier protein Aralar2 (SLC25A13) ELISA Kit

Secondary Antibody

Anti-HRP Goat Anti-Rabbit IgG (H+L) Antibody (CABS014)