Fatty Acid Transport Protein 4 (FATP4), 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 FATP4 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.

MBS9375394 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Fatty Acid Transport Protein 4 (FATP4) 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 FATP4. The ELISA analytical biochemical technique of the MBS9375394 kit is based on FATP4 antibody-FATP4 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect FATP4 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, FATP4. 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(%).

72,319 Da

solute carrier family 27 (fatty acid transporter), member 4

long-chain fatty acid transport protein 4

Long-chain fatty acid transport protein 4

Acsvl4; Fatp4; FATP-4; Fatty acid transport protein 4  [Similar Products]

S27A4_MOUSE

SLC27A4: Involved in translocation of long-chain fatty acids (LFCA) across the plasma membrane. Appears to be the principal fatty acid transporter in small intestinal enterocytes. Plays a role in the formation of the epidermal barrier. Required for fat absorption in early embryogenesis. Has acyl-CoA ligase activity for long-chain and very-long-chain fatty acids. Defects in SLC27A4 are the cause of ichthyosis prematurity syndrome (IPS). A keratinization disorder characterized by complications in the second trimester of pregnancy resulting from polyhydramnion, with premature birth of a child with thick caseous desquamating epidermis, respiratory complications and transient eosinophilia. After recovery during the first months of life, the symptoms are relatively benign and the patients suffer from a lifelong non-scaly ichthyosis with atopic manifestations. Belongs to the ATP-dependent AMP-binding enzyme family.

Protein type: Transporter, SLC family; EC 6.2.1.-; Membrane protein, multi-pass; Ligase; Transporter; Membrane protein, integral

Cellular Component: brush border membrane; endoplasmic reticulum; endoplasmic reticulum membrane; membrane; microvillus; plasma membrane

Molecular Function: long-chain-fatty-acid-CoA ligase activity; very-long-chain-fatty-acid-CoA ligase activity

Biological Process: fatty acid metabolic process; long-chain fatty acid metabolic process; long-chain fatty acid transport; medium-chain fatty acid transport; skin development; very-long-chain fatty acid catabolic process; very-long-chain fatty acid metabolic process

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