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SLC22A5, Polyclonal Antibody

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产品名称: SLC22A5, Polyclonal Antibody
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简单介绍

SLC22A5, Polyclonal Antibody


SLC22A5, Polyclonal Antibody  的详细介绍
Product Name

SLC22A5, Polyclonal Antibody

Full Product Name

SLC22A5 Antibody

Product Gene Name

anti-SLC22A5 antibody

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
AF057164 mRNA
3D Structure
ModBase 3D Structure for O76082
Clonality
Polyclonal
Host
Rabbit
Species Reactivity
Human
Specificity
SLC22A5 Antibody detects endogenous levels of SLC22A5.
Purity/Purification
Purified from rabbit antiserum by affinity-chromatography using immunogen.
Form/Format
Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Concentration
1 mg/ml (lot specific)
Target Modification
Unmodified/Total
Immunogen
The antiserum was produced against synthesized peptide derived from human SLC22A5.
Immunogen Range
282-331
Preparation and Storage
Stable at -20 degree C for at least 1 year.
Other Notes
Small volumes of anti-SLC22A5 antibody 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.
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Applications Tested/Suitable for anti-SLC22A5 antibody
Western Blot (WB), ELISA (EIA)
Application Notes for anti-SLC22A5 antibody
WB: 1:500~1:1000
ELISA: 1:10000

Western Blot (WB) of anti-SLC22A5 antibody
Western blot analysis of the lysates from HeLa cells using SLC22A5 antibody.
anti-SLC22A5 antibody Western Blot (WB) (WB) image
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NCBI/Uniprot data below describe general gene information for SLC22A5. It may not necessarily be applicable to this product.
NCBI GI #
815890826
NCBI GeneID
6584
NCBI Accession #
NP_001295051.1 [Other Products]
NCBI GenBank Nucleotide #
NM_001308122.1 [Other Products]
UniProt Primary Accession #
O76082 [Other Products]
UniProt Secondary Accession #
Q6ZQZ8; Q96EH6; A2Q0V1; B2R844; D3DQ87[Other Products]
UniProt Related Accession #
O76082[Other Products]
Molecular Weight
62 kDa
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NCBI Official Full Name
solute carrier family 22 member 5 isoform a
NCBI Official Synonym Full Names
solute carrier family 22 member 5
NCBI Official Symbol
SLC22A5  [Similar Products]
NCBI Official Synonym Symbols
CDSP; OCTN2
  [Similar Products]
NCBI Protein Information
solute carrier family 22 member 5
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  [Similar Products]
UniProt Synonym Gene Names
OCTN2  [Similar Products]
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NCBI Summary for SLC22A5
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. [provided by RefSeq, Apr 2015]
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UniProt Comments for 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.
Research Articles on SLC22A5
1. The OCTN2 carnitine transporter is essential for retaining carnitine in the body and allowing adequate supplies to the heart and the skeletal muscle, which derive most of their energy from fat. Mutations impairing its function result in carnitine deficiency that can present early in life with hypoketotic hypoglycemia, or later in life with cardiomyopathy and sudden death from cardiac arrhythmia. Review.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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