GeneBio Systems
Anti-Spermine synthase/SMS Antibody Picoband®
Anti-Spermine synthase/SMS Antibody Picoband®
SKU:A01831-1
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Size: 100 μg
Storage: At -20℃ for one year from date of receipt. After reconstitution, at 4℃ for one month. It can also be aliquotted and stored frozen at -20℃ for six months. Avoid repeated freezing and thawing.
Form: Lyophilized
Reactivity: Human
Applications: WB,Flow Cytometry,ELISA
Application Details: Western blot, 0.25-0.5 μg/ml, Human
Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
ELISA, 0.1-0.5 μg/ml, -
Gene Name: SMS
Specificity:
Background: This gene encodes a protein belonging to the spermidine/spermin synthase family and catalyzes the production of spermine from spermidine. Pseudogenes of this gene are located on chromosomes 1, 5, 6 and X. Mutations in this gene cause an X-linked intellectual disability called Snyder-Robinson Syndrome (SRS). Multiple transcript variants encoding different isoforms have been found for this gene.
Immunogen: E.coli-derived human Spermine synthase/SMS recombinant protein (Position: Q102-K365).
Clonality: Polyclonal
Contents: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
Purification: Immunogen affinity purified.
Reconstitution: Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
Reference: 1. Becerra-Solano, L. E., Butler, J., Castaneda-Cisneros, G., McCloskey, D. E., Wang, X., Pegg, A. E., Schwartz, C. E., Sanchez-Corona, J., Garcia-Ortiz, J. E. A missense mutation, p.V132G, in the X-linked spermine synthase gene (SMS) causes Snyder-Robinson syndrome. Am. J. Med. Genet. 149A: 328-335, 2009. 2. Cason, A. L., Ikeguchi, Y., Skinner, C., Wood, T. C., Holden, K. R., Lubs, H. A., Martinez, F., Simensen, R. J., Stevenson, R. E., Pegg, A. E., Schwartz, C. E. X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome. Europ. J. Hum. Genet. 11: 937-944, 2003. 3. de Alencastro, G., McCloskey, D. E., Kliemann, S. E., Maranduba, C. M. C., Pegg, A. E., Wang, X., Bertola, D. A., Schwartz, C. E., Passos-Bueno, M. R., Sertie, A. L. New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome. (Letter) J. Med. Genet. 45: 539-543, 2008.
Uniprot ID: P52788
Host: Rabbit
Concentration: Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
Conjugate:
Cross Reactivity: No cross-reactivity with other proteins.
Isotype: Rabbit IgG
Phospho_site:
Clone Number:
Observed Molecular Weight: 41 kDa
Calculated Molecular Weight: 18080 MW
Gene ID: 6611
Protein Name: Spermine synthase
Gene Full Name: spermine synthase
Synonyms: MRSR; SMS; Spermine synthase; SPMSY; SpS
