Anti-Slc7a9 Antibody Picoband® Fluoro647 Conjugated
Product Specifications
Background
B (0, +) -type amino acid transporter 1, also known as b (0, +) AT1, is a protein which in humans is encoded by the SLC7A9 gene. This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Alternate transcript variants, which encode the same protein, have been found for this gene.
Synonyms
Pulmonary surfactant-associated protein B; SP-B; 18 kDa pulmonary-surfactant protein; 6 kDa protein; Pulmonary surfactant-associated proteolipid SPL (Phe) ; SFTPB; SFTP3
Gene Name
Slc7a9
Gene ID
30962
UniProt
Q9QXA6
Host
Rabbit
Reactivity
Mouse, Rat
Cross Reactivity
No cross-reactivity with other proteins.
Immunogen
E.coli-derived mouse Slc7a9 recombinant protein (Position: M1-E487) .
Clonality
Polyclonal
Tissue Specificity
Found in the synovial fluid of patients with rheumatoid arthritis. .
Applications
Flow Cytometry
Field of Research
Cancer, Cardiovascular, Cell Biology, Cell Cycle, Cell Differentiation, Lipases, Lipid and Lipoprotein Metabolism, Lipid Metabolism, Lipids/Lipoproteins, Metabolic Signaling Pathways, Metabolism, Pathways and Processes, Signal Transduction, Vasculature
Purification
Immunogen affinity purified.
Form
Liquid
Function
Pulmonary surfactant-associated proteins promote alveolar stability by lowering the surface tension at the air- liquid interface in the peripheral air spaces. SP-B increases the collapse pressure of palmitic acid to nearly 70 millinewtons per meter.
References & Citations
1. Brodehl, J., Gellissen, K., Kowalewski, S. Isolierter Defekt der tubulaeren Cystin-Rueckresorption in einer Familie mit idiopathischem Hypoparathyroidismus. Klin. Wschr. 45: 38-40, 1967. 2. Colombo, R. Dating the origin of the V170M mutation causing non-type I cystinuria in Libyan Jews by linkage disequilibrium and physical mapping of the SLC7A9 gene. Genomics 69: 131-134, 2000. 3. Dello Strologo, L., Pras, E., Pontesilli, C., Beccia, E., Ricci-Barbini, V., de Sanctis, L., Ponzone, A., Gallucci, M., Bisceglia, L., Zelante, L., Jimenez-Vidal, M., Font, M., Zorzano, A., Rousaud, F., Nunes, V., Gasparini, P., Palacin, M., Rizzoni, G. Comparison between SLC3A1 and SLC7A9 cystinuria patients and carriers: a need for a new classification. J. Am. Soc. Nephrol. 13: 2547-2553, 2002.
Storage Conditions
At -20 ̊C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
Product Datasheet
https://www.bosterbio.com/datasheet?sku=A03445-1-Fluoro647
Calculated Molecular Weight
31203 MW
Applications Notes
6
Gene Name Synonym
Surfactant protein B
Subcellular Location
Secreted, extracellular space, surface film.
Protein Name
Tumor necrosis factor-inducible gene 6 protein
Isotype
Rabbit IgG
Contents
Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.
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