Anti-SLC22A5 抗体 (CAB1676)

抗体名:	Anti-SLC22A5 Antibody
抗体コード:	CAB1676
抗体サイズ:	20uL, 50uL, 100uL
申し込み:	WB IF
反応性:	Human, Mouse, Rat
宿主種:	Rabbit
免疫原:	Recombinant fusion protein containing a sequence corresponding to amino acids 1-180 of human SLC22A5 (NP_003051.1).

申し込み:	WB IF
推奨希釈:	WB 1:500 - 1:2000 IF 1:50 - 1:200
反応性:	Human, Mouse, Rat
ポジティブサンプル:	MCF7, OVCAR3, A-549, DU145, SW480, Mouse intestine, Mouse kidney

免疫原:	Recombinant fusion protein containing a sequence corresponding to amino acids 1-180 of human SLC22A5 (NP_003051.1).
精製方法:	Affinity purification
ストレージバッファ:	Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
アイソタイプ:	IgG
順序:	MRDY DEVT AFLG EWGP FQRL IFFL LSAS IIPN GFTG LSSV FLIA TPEH RCRV PDAA NLSS AWRN HTVP LRLR DGRE VPHS CRRY RLAT IANF SALG LEPG RDVD LGQL EQES CLDG WEFS QDVY LSTI VTEW NLVC EDDW KAPL TISL FFVG VLLG SFIS GQLS DRFG RKNV LFVT MGMQ
遺伝子ID:	6584
Uniprot:	O76082
セルラーロケーション:	Membrane, Multi-pass membrane protein
計算された分子量:	24kDa/62kDa/65kDa
観察された分子量:	70kDa

同義語:

SLC22A5, CDSP, OCTN2

バックグラウンド:

Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy. Alternative splicing of this gene results in multiple transcript variants.

UniProt Protein Function:	SLC22A5: Sodium-ion dependent, high affinity carnitine transporter. Involved in the active cellular uptake of carnitine. Transports one sodium ion with one molecule of carnitine. Also transports organic cations such as tetraethylammonium (TEA) without the involvement of sodium. Also relative uptake activity ratio of carnitine to TEA is 11.3. Defects in SLC22A5 are the cause of systemic primary carnitine deficiency (CDSP). CDSP is an autosomal recessive disorder of fatty acid oxidation caused by defective carnitine transport. Present early in life with hypoketotic hypoglycemia and acute metabolic decompensation, or later in life with skeletal myopathy or cardiomyopathy. Belongs to the major facilitator (TC 2.A.1) superfamily. Organic cation transporter (TC 2.A.1.19) family. 3 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:	Protein type:Transporter, SLC family; Membrane protein, multi-pass; Membrane protein, integral; Transporter Chromosomal Location of Human Ortholog: 5q23.3 Cellular Component: brush border membrane; basolateral plasma membrane; apical plasma membrane; plasma membrane; integral to membrane Molecular Function:protein binding; antibiotic transporter activity; symporter activity; carnitine transporter activity; drug transporter activity; quaternary ammonium group transmembrane transporter activity; ATP binding; PDZ domain binding Biological Process: quaternary ammonium group transport; drug transport; antibiotic transport; sodium ion transport; multidrug transport; transmembrane transport; carnitine transport; quorum sensing during interaction with host Disease: Carnitine Deficiency, Systemic Primary
NCBI Summary:	Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy. [provided by RefSeq, Jul 2008]
UniProt Code:	O76082
NCBI GenInfo Identifier:	8928257
NCBI Gene ID:	6584
NCBI Accession:	O76082.1
UniProt Secondary Accession:	O76082,Q6ZQZ8, Q96EH6, A2Q0V1, B2R844, D3DQ87,
UniProt Related Accession:	O76082
Molecular Weight:	557
NCBI Full Name:	Solute carrier family 22 member 5
NCBI Synonym Full Names:	solute carrier family 22 (organic cation/carnitine transporter), member 5
NCBI Official Symbol:	SLC22A5
NCBI Official Synonym Symbols:	CDSP; OCTN2; OCTN2VT
NCBI Protein Information:	solute carrier family 22 member 5; organic cation/carnitine transporter 2; high-affinity sodium dependent carnitine cotransporter
UniProt Protein Name:	Solute carrier family 22 member 5
UniProt Synonym Protein Names:	High-affinity sodium-dependent carnitine cotransporter; Organic cation/carnitine transporter 2
Protein Family:	Solute carrier family
UniProt Gene Name:	SLC22A5
UniProt Entry Name:	S22A5_HUMAN

	Western blot analysis of extracts of various cell lines, using SLC22A5 antibody (CAB1676) 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.
	Immunofluorescence analysis of MCF-7 cells using SLC22A5 antibody (CAB1676). Blue: DAPI for nuclear staining.

Antibodies

Anti-SLC22A5 Antibody (CAB14785)

SLC22A5 Antibody (PACO05089)

SLC22A5 Antibody (PACO12256)

Secondary Antibody

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