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SLC16A1 elisa kit :: Canine Solute Carrier Family 16, Member 1 (SLC16A1) ELISA Kit

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Catalog # MBS9388273
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SLC16A1 elisa kit
Product Name

Solute Carrier Family 16, Member 1 (SLC16A1), ELISA Kit

Popular Item
Full Product Name

Canine Solute Carrier Family 16, Member 1 (SLC16A1) ELISA Kit

Product Gene Name
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
OMIM
L31801 mRNA
Species Reactivity
Preparation and Storage
Store all reagents at 2-8 degree C
Product Note
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 SLC16A1 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 SLC16A1purchase
MBS9388273 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Solute Carrier Family 16, Member 1 (SLC16A1) 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 SLC16A1. The ELISA analytical biochemical technique of the MBS9388273 kit is based on SLC16A1 antibody-SLC16A1 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect SLC16A1 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, SLC16A1. 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 SLC16A1. It may not necessarily be applicable to this product.
NCBI GI #
NCBI GeneID
NCBI Accession #
UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
46,234 Da
NCBI Official Full Name
solute carrier family 16 (monocarboxylic acid transporters), member 1, isoform CRA_b
NCBI Official Synonym Full Names
solute carrier family 16 member 1
NCBI Official Symbol
SLC16A1  [Similar Products]
NCBI Official Synonym Symbols
MCT; HHF7; MCT1; MCT1D
  [Similar Products]
NCBI Protein Information
monocarboxylate transporter 1
UniProt Protein Name
Monocarboxylate transporter 1
UniProt Synonym Protein Names
Solute carrier family 16 member 1
UniProt Gene Name
SLC16A1  [Similar Products]
UniProt Synonym Gene Names
MCT1; MCT 1  [Similar Products]
NCBI Summary for SLC16A1
The protein encoded by this gene is a proton-linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2009]
UniProt Comments for SLC16A1
MCT1: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate. Defects in SLC16A1 are the cause of symptomatic deficiency in lactate transport (SDLT); also known as erythrocyte lactate transporter defect. Deficiency of lactate transporter may result in an acidic intracellular environment created by muscle activity with consequent degeneration of muscle and release of myoglobin and creatine kinase. This defect might compromise extreme performance in otherwise healthy individuals. Defects in SLC16A1 are the cause of familial hyperinsulinemic hypoglycemia type 7 (HHF7); also known as exercise-induced hyperinsulinemic hypoglycemia. HHF7 is a dominantly inherited hypoglycemic disorder characterized by inappropriate insulin secretion during anaerobic exercise or on pyruvate load. Belongs to the major facilitator superfamily. Monocarboxylate porter (TC 2.A.1.13) family.

Protein type: Membrane protein, integral; Membrane protein, multi-pass; Mitochondrial; Transporter; Transporter, SLC family

Chromosomal Location of Human Ortholog: 1p13.2

Cellular Component: centrosome; integral to membrane; integral to plasma membrane; membrane; plasma membrane

Molecular Function: lactate transmembrane transporter activity; mevalonate transmembrane transporter activity; monocarboxylic acid transmembrane transporter activity

Biological Process: centrosome organization and biogenesis; leukocyte migration; mevalonate transport; monocarboxylic acid transport; pyruvate metabolic process

Disease: Erythrocyte Lactate Transporter Defect; Hyperinsulinemic Hypoglycemia, Familial, 7; Monocarboxylate Transporter 1 Deficiency
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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