Anoctamin 6 (ANO6), ELISA Kit

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

Store all reagents at 2-8 degree C

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Small volumes of ANO6 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.

MBS9375942 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Anoctamin 6 (ANO6) 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 ANO6. The ELISA analytical biochemical technique of the MBS9375942 kit is based on ANO6 antibody-ANO6 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect ANO6 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, ANO6. 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(%).

108,102 Da

anoctamin 6

anoctamin-6

Anoctamin-6

TMEM16F; SCAN channel  [Similar Products]

ANO6_HUMAN

This gene encodes a multi-pass transmembrane protein that belongs to the anoctamin family. This protein is an essential component for the calcium-dependent exposure of phosphatidylserine on the cell surface. The scrambling of phospholipid occurs in various biological systems, such as when blood platelets are activated, they expose phosphatidylserine to trigger the clotting system. Mutations in this gene are associated with Scott syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2011]

ANO6: May act as a calcium-activated chloride channel. It is essential for calcium-dependent exposure of phosphatidylserine on the surface of activated platelets, a process necessary to trigger the clotting system. Defects in ANO6 are the cause of Scott syndrome (SCTS). A mild bleeding disorder due to impaired surface exposure of procoagulant phosphatidylserine (PS) on platelets and other blood cells, following activation with Ca(2+)-elevating agents. Belongs to the anoctamin family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Transporter, ion channel; Transporter; Membrane protein, integral; Membrane protein, multi-pass

Chromosomal Location of Human Ortholog: 12q12

Cellular Component: cell surface; intracellular; membrane; plasma membrane

Molecular Function: calcium activated cation channel activity; intracellular calcium activated chloride channel activity; protein binding; voltage-gated chloride channel activity; voltage-gated ion channel activity

Biological Process: activation of blood coagulation via clotting cascade; bleb formation; blood coagulation; cation transport; chloride transport; negative regulation of cell volume; phospholipid scrambling; pore complex biogenesis; positive regulation of apoptosis; positive regulation of bone mineralization; positive regulation of phagocytosis, engulfment

Disease: Scott Syndrome

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