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SLC7A1 Antibody (C-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| WB, E |
|---|---|
| Primary Accession | P30825 |
| Other Accession | NP_003036.1 |
| Reactivity | Human |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 67638 Da |
| Antigen Region | 429-457 aa |
| Gene ID | 6541 |
|---|---|
| Other Names | High affinity cationic amino acid transporter 1, CAT-1, CAT1, Ecotropic retroviral leukemia receptor homolog, Ecotropic retrovirus receptor homolog, ERR, Solute carrier family 7 member 1, System Y+ basic amino acid transporter, SLC7A1, ATRC1, ERR, REC1L |
| Target/Specificity | This SLC7A1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 429-457 amino acids from the C-terminal region of human SLC7A1. |
| Dilution | WB~~1:1000 |
| Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
| Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
| Precautions | SLC7A1 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
| Name | SLC7A1 (HGNC:11057) |
|---|---|
| Function | High-affinity, low capacity permease involved in the transport of the cationic amino acids (arginine, lysine and ornithine) in non-hepatic tissues. |
| Cellular Location | Cell membrane {ECO:0000250|UniProtKB:Q09143}; Multi-pass membrane protein |
| Tissue Location | Ubiquitous.. |
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Provided below are standard protocols that you may find useful for product applications.
Background
High-affinity, low capacity permease involved in the transport of the cationic amino acids (arginine, lysine and ornithine) in non-hepatic tissues. May also function as an ecotropic retroviral leukemia receptor.
References
Yang, Z., et al. Hum. Mutat. 30(3):328-333(2009)
Jaeger, K., et al. Histochem. Cell Biol. 129(3):321-329(2008)
Broer, S. Physiol. Rev. 88(1):249-286(2008)
Maeda, T., et al. Drug Metab. Pharmacokinet. 23(3):181-187(2008)
Kaneko, S., et al. Am. J. Physiol., Cell Physiol. 293 (2), C729-C737 (2007) :
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