| SMPD1 Rabbit mAb |
| LTA24771 |
| 100ul |
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$750
In stock
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| The protein encoded by this gene is a lysosomal acid sphingomyelinase that converts sphingomyelin to ceramide. The encoded protein also has phospholipase C activity. Defects in this gene are a cause of Niemann-Pick disease type A (NPA) and Niemann-Pick disease type B (NPB). Multiple transcript variants encoding different isoforms have been identified. |
| ASM; NPD; ASMASE |
| 6609,ASM,SMPD1,ASMASE,NPD,sphingomyelin phosphodiesterase 1,sphingomyelin phosphodiesterase,acid sphingomyelinase,acid lysosomal,P17405,Sphingomyelin Phosphodiesterase 1,Acid Sphingomyelinase,Acid Lysosomal,Sphingomyelin Phosphodiesterase,EC 3.1.4.12,ASMase,SMPD1/ASM |
| Human |
| 6609 |
| P17405 |
| PARLHRIVPRLRDVFGWGNLTCPICKGLFTAINLGLKKEPNVARVGSVAIKLCNLLKIAPPAVCQSIVHLFEDDMVEVWRRSVLSPSEACGLLLGSTCGHWDIFSSWNISLPTVPKPPPKPPSPPAPGAPVSRILFLTDLHWDHDYLEGTDPDCADPLCCRRGSGLPPASRPGAGYWGEYSKCDLPLRTLESLLSGLGPAGPFDMVYWTGDIPAHDVWHQTRQDQLRALTTVTALVRKFLGPVPVYPAVGNHESTPVNSFPPPFIEGNHSS |
| Recombinant fusion protein containing a sequence corresponding to amino acids 70-340 of human SMPD1 (NP_000534.3). |
| Rabbit |
| Affinity Purified Monoclonal IgG |
| IHC-P, ELISA |
| Human, Mouse, Rat |
| 70kDa |
| IHC-P,1:200 - 1:2000|ELISA,Recommended starting concentration is 1 _g/mL. Please optimize the concentration based on your specific assay requirements. |
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Reconstituted antibodies stable at -80C for 12 months, 4C for 1 week. Avoid repeated freeze-thaw cycles.
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Shipped at ambient temperature.
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Centrifuge tubes before opening. Dissolve the lyophilized antibodies in distilled water. 5-10% glycerol is recommended.
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Immunohistochemistry analysis of paraffin-embedded Human liver tissue using SMPD1 Rabbit mAb (LTA24771) at a dilution of 1:300 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining. |