Product Name
Solute Carrier Family 22 Member 5 (SLC22A5), ELISA Kit
Full Product Name
Donkey Solute Carrier Family 22 Member 5 (SLC22A5) ELISA Kit
Product Gene Name
SLC22A5 elisa kit
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
Request Current Manual
Species Reactivity
Donkey
Preparation and Storage
Store all reagents at 2-8 degree C
Product Note
Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of SLC22A5 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Searchable Terms for SLC22A5 purchase
MBS9348455 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Solute Carrier Family 22 Member 5 (SLC22A5) ELISA Kit target analytes in
biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing SLC22A5. The ELISA analytical biochemical technique of the MBS9348455 kit is based on SLC22A5 antibody-SLC22A5 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect SLC22A5 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, SLC22A5. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
NCBI/Uniprot data below describe general gene information for SLC22A5. It may not necessarily be applicable to this product.
NCBI Accession #
NP_062142.1
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NCBI GenBank Nucleotide #
NM_019269.1
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UniProt Secondary Accession #
Q9QWL0[Other Products]
UniProt Related Accession #
O70594[Other Products]
Molecular Weight
62,567 Da
NCBI Official Full Name
solute carrier family 22 member 5
NCBI Official Synonym Full Names
solute carrier family 22 member 5
NCBI Official Symbol
Slc22a5 [Similar Products]
NCBI Official Synonym Symbols
CT1; OCTN2; UST2r
[Similar Products]
NCBI Protein Information
solute carrier family 22 member 5
UniProt Protein Name
Solute carrier family 22 member 5
UniProt Synonym Protein Names
CT1; High-affinity sodium-dependent carnitine cotransporter; Organic cation/carnitine transporter 2; UST2r
Protein Family
Solute carrier family
UniProt Gene Name
Slc22a5 [Similar Products]
UniProt Synonym Gene Names
Octn2 [Similar Products]
UniProt Entry Name
S22A5_RAT
NCBI Summary for SLC22A5
mediates high-affinity sodium-dependent carnitine transport and sodium-independent organic cation transport [RGD, Feb 2006]
UniProt Comments for SLC22A5
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.
Protein type: Transporter; Membrane protein, integral; Transporter, SLC family; Membrane protein, multi-pass
Cellular Component: apical plasma membrane; basolateral plasma membrane; brush border membrane; integral to membrane; integral to plasma membrane; mitochondrion
Molecular Function: antibiotic transporter activity; ATP binding; carnitine transporter activity; cation:cation antiporter activity; PDZ domain binding; protein binding; quaternary ammonium group transmembrane transporter activity; symporter activity; transmembrane transporter activity
Biological Process: ***** heart development; antibiotic transport; carnitine metabolic process; carnitine transport; locomotory behavior; mitochondrion organization and biogenesis; quaternary ammonium group transport; quorum sensing during interaction with host; reproductive structure development; sodium ion transport; transmembrane transport; triacylglycerol metabolic process
Research Articles on SLC22A5
1. PKC activation resulted in an augmented Octn2 presence in cholesterol/sphingolipid-rich microdomains of plasma membrane (rafts) and increased co-precipitation of Octn2 with raft-proteins, caveolin-1 and flotillin-1.
Precautions
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Disclaimer
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