LAT1 Antibody #5347
Filter:
- WB
- IP
Supporting Data
REACTIVITY | H |
SENSITIVITY | Endogenous |
MW (kDa) | 39 |
SOURCE | Rabbit |
Application Key:
- WB-Western Blotting
- IP-Immunoprecipitation
Species Cross-Reactivity Key:
- H-Human
Product Information
Product Usage Information
Application | Dilution |
---|---|
Western Blotting | 1:1000 |
Immunoprecipitation | 1:100 |
Storage
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA and 50% glycerol. Store at –20°C. Do not aliquot the antibody.
Protocol
Specificity / Sensitivity
LAT1 Antibody detects endogenous levels of total LAT1 protein.
Species Reactivity:
Human
Source / Purification
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues at the amino terminus of human LAT1 protein. Antibodies were purified by protein A and peptide affinity chromatography.
Background
L-type amino acid transporter 1 (LAT1), also known as solute carrier family 7 member 5 (SLC7A5), is a high-affinity neutral transporter of larger amino acids. It facilitates the cellular amino acid uptake in a sodium independent manner (1-2) and selectively transports D-and L-isomers of small neutral amino acids (3). LAT1 also regulates amino acid exchange in conjunction with solute carrier family 1 member 5 (SLC1A5) (2,4-6). Transport of thyroid hormones across the placenta is established via LAT1 during normal fetal development (7). LAT1 promotes neuronal cell proliferation by regulating the transport of amino acids across the blood brain barrier (8). LAT1 is upregulated in various cancer types, including breast cancer, lung cancer, prostate cancer, and gliomas (9,10). High expression of LAT1 is detected in non-small cell lung cancer with lymph node metastases (9,11,12). Increased LAT1 expression is a novel biomarker of high grade malignancy in prostate cancers (12). Inhibition of LAT1 suppresses tumor cell growth in several tumor types (10,13).
- Mastroberardino, L. et al. (1998) Nature 395, 288-91.
- Kanai, Y. et al. (1998) J Biol Chem 273, 23629-32.
- Torrents, D. et al. (1998) J Biol Chem 273, 32437-45.
- Meier, C. et al. (2002) EMBO J 21, 580-9.
- Yanagida, O. et al. (2001) Biochim Biophys Acta 1514, 291-302.
- Nicklin, P. et al. (2009) Cell 136, 521-34.
- Ritchie, J.W. and Taylor, P.M. (2001) Biochem J 356, 719-25.
- Verrey, F. (2003) Pflugers Arch 445, 529-33.
- Kaira, K. et al. (2009) Ann Surg Oncol 16, 3473-81.
- Kobayashi, K. et al. (2008) Neurosurgery 62, 493-503; discussion 503-4.
- Imai, H. et al. (2009) Histopathology 54, 804-13.
- Sakata, T. et al. (2009) Pathol Int 59, 7-18.
- Shennan, D.B. and Thomson, J. (2008) Oncol Rep 20, 885-9.
限制使用
除非 CST 的合法授书代表以书面形式书行明确同意,否书以下条款适用于 CST、其关书方或分书商提供的书品。 任何书充本条款或与本条款不同的客书条款和条件,除非书 CST 的合法授书代表以书面形式书独接受, 否书均被拒书,并且无效。
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For Research Use Only. Not For Use In Diagnostic Procedures.
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