SLC27A4 Antibody (C-term) Blocking Peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | Q6P1M0 |
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Clone Names | 100405053 |
Gene ID | 10999 |
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Other Names | Long-chain fatty acid transport protein 4, FATP-4, Fatty acid transport protein 4, 621-, Solute carrier family 27 member 4, SLC27A4, ACSVL4, FATP4 |
Target/Specificity | The synthetic peptide sequence used to generate the antibody AP13227b was selected from the C-term region of SLC27A4. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay. |
Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
Name | SLC27A4 (HGNC:10998) |
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Function | Mediates the levels of long-chain fatty acids (LCFA) in the cell by facilitating their transport across cell membranes (PubMed:10518211, PubMed:12556534, PubMed:20448275, PubMed:21395585, PubMed:22022213). Appears to be the principal fatty acid transporter in small intestinal enterocytes (PubMed:20448275). Also functions as an acyl-CoA ligase catalyzing the ATP-dependent formation of fatty acyl- CoA using LCFA and very-long-chain fatty acids (VLCFA) as substrates, which prevents fatty acid efflux from cells and might drive more fatty acid uptake (PubMed:22022213, PubMed:24269233). Plays a role in the formation of the epidermal barrier. Required for fat absorption in early embryogenesis (By similarity). Probably involved in fatty acid transport across the blood barrier (PubMed:21395585). Indirectly inhibits RPE65 via substrate competition and via production of VLCFA derivatives like lignoceroyl-CoA. Prevents light-induced degeneration of rods and cones (By similarity). |
Cellular Location | Endoplasmic reticulum membrane; Multi-pass membrane protein |
Tissue Location | Expressed at highest levels in brain, testis, colon and kidney. Expressed at medium levels in heart and liver, small intestine and stomach. Expressed at low levels in peripheral leukocytes, bone marrow, skeletal muscle and aorta. Expressed in adipose tissue (PubMed:24269233, PubMed:9878842). Expressed in brain gray matter (PubMed:21395585). |
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes a member of a family of fatty acidtransport proteins, which are involved in translocation oflong-chain fatty acids cross the plasma membrane. This protein isexpressed at high levels on the apical side of mature enterocytesin the small intestine, and appears to be the principal fatty acidtransporter in enterocytes. Clinical studies suggest this gene as acandidate gene for the insulin resistance syndrome. Mutations inthis gene have been associated with ichthyosis prematuritysyndrome.
References
Morice-Picard, F., et al. Am. J. Med. Genet. A 152A (10), 2664-2665 (2010) :Yokoyama, K., et al. Nephron Clin Pract 115 (4), C237-C243 (2010) :Ban, H.J., et al. BMC Genet. 11, 26 (2010) :Klar, J., et al. Am. J. Hum. Genet. 85(2):248-253(2009)Jia, Z., et al. J. Mol. Neurosci. 33(1):25-31(2007)
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