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Conjugation/Formulation：Un-conjugated
- Background The protein encoded by this intronless gene is an endothelial-specific type I membrane receptor that binds thrombin. This binding results in the activation of protein C, which degrades clotting factors Va and VIIIa and reduces the amount of thrombin generated. Mutations in this gene are a cause of thromboembolic disease, also known as inherited thrombophilia. [provided by RefSeq, Jul 2008]
- Immunogen A synthetic peptide of human Thrombomodulin
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Gene ID
7056
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Swiss Prot
P07204
- Synonyms TM; THRM; AHUS6; BDCA3; CD141; THPH12
- Reactivity Human
- Application WB, IHC-P, ICC/IF, FC, IP
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Recommended dilution
WB: 1:1000-1:5000
IHC-P: 1:100-1:1000
ICC/IF: 1:100-1:200
FC: 1:20-1:50
IP: 1:10-1:100 - Calculated MW 60 kDa
- Observed MW 95 kDa
- Host species Rabbit
- Clonality Monoclonal
- Clonality No. DGR11524
- 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 Thrombomodulin in Jurkat cell lysates using Thrombomodulin antibody(1:1000 diluted). -
Immunofluorescent analysis of A549 cells using db11952 antibody (green), and DAPI (blue).
订购信息
- Package Price (RMB)
- 10μL 398
- 20μL 698
- 50μL 1398
- 100μL 2398
- 货期：现货
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For research use only. Not intended for diagnostic.
