For Research Use Only. Not for use in diagnostic procedures.

This assay has high sensitivity and excellent specificity for detection of Horse SCN4A. No significant cross-reactivity or interference between Horse SCN4A and analogues was observed.

Store at 2-8 degree C.

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.

Small volumes of SCN4A 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.

MBS281539 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Sodium channel protein type 4 subunit alpha (SCN4A) 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 SCN4A. The ELISA analytical biochemical technique of the MBS281539 kit is based on SCN4A antibody-SCN4A antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect SCN4A antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, SCN4A. 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(%).

Principle of the Assay: This assay employs a two-site sandwich ELISA to quantitate SCN4A in samples. An antibody specific for SCN4A has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anySCN4A present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for SCN4A is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of SCN4A bound in the initial step. The color development is stopped and the intensity of the color is measured.

207,487 Da

sodium voltage-gated channel alpha subunit 4

sodium channel protein type 4 subunit alpha; LOW QUALITY PROTEIN: sodium channel protein type 4 subunit alpha

Sodium channel protein type 4 subunit alpha

This protein mediates the voltage-dependent sodium ion permeability of excitable membranes. Assuming opened or closed conformations in response to the voltage difference across the membrane, the protein forms a sodium-selective channel through which Na+ ions may pass in accordance with their electrochemical gradient. This sodium channel may be present in both denervated and innervated skeletal muscle.

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