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Spermine synthase (DGR19135) Rabbit mAb
db12119
Datasheet
- 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. [provided by RefSeq, Jul 2017]
- Immunogen A synthetic peptide of human Spermine synthase
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Gene ID
6611
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Swiss Prot
P52788
- Synonyms SRS; SpS; MRSR; SPMSY
- Reactivity Human,Mouse,Rat
- Application WB, ICC/IF
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Recommended dilution
WB: 1:1000-1:5000
ICC/IF: 1:200-1:500 - Calculated MW 41 kDa
- Observed MW 41 kDa
- Host species Rabbit
- Clonality Monoclonal
- Clonality No. DGR19135
- Isotype IgG
- Purity Affinity Purification
- Conjugation Un-conjugated
- Storage/Stability Store at -20°C. Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.
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Western blot detection of Spermine synthase in K562,Hela cell lysates using Spermine synthase antibody(1:1000 diluted).
订购信息
- Package Price (RMB)
- 10μL 398
- 20μL 698
- 50μL 1398
- 100μL 2398
- 货期：现货
相关产品
For research use only. Not intended for diagnostic.
