SMPD1 anticorps (Middle Region)
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- Antigène Voir toutes SMPD1 Anticorps
- SMPD1 (Sphingomyelin phosphodiesterase 1, Acid Lysosomal (SMPD1))
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Épitope
- Middle Region
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Reactivité
- Humain, Souris, Rat, Boeuf (Vache), Mouton, Lapin, Chien, Cheval, Cobaye
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp SMPD1 est non-conjugé
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Application
- Western Blotting (WB)
- Séquence
- RLRDVFGWGN LTCPICKGLF TAINLGLKKE PNVARVGSVA IKLCNLLKIA
- Homologie
- Cow: 83%, Dog: 87%, Guinea Pig: 87%, Horse: 80%, Human: 100%, Mouse: 80%, Rabbit: 87%, Rat: 87%, Sheep: 83%
- Attributs du produit
- This is a rabbit polyclonal antibody against SMPD1. It was validated on Western Blot.
- Purification
- Affinity Purified
- Immunogène
- The immunogen is a synthetic peptide directed towards the middle region of human SMPD1
- Top Product
- Discover our top product SMPD1 Anticorps primaire
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- Indications d'application
- Optimal working dilution should be determined by the investigator.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Conseil sur la manipulation
- Avoid repeat freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- Antigène
- SMPD1 (Sphingomyelin phosphodiesterase 1, Acid Lysosomal (SMPD1))
- Autre désignation
- SMPD1 (SMPD1 Produits)
- Synonymes
- anticorps ASM, anticorps ASMASE, anticorps NPD, anticorps A-SMase, anticorps Zn-SMase, anticorps aSMase, anticorps SMPD1, anticorps sphingomyelin phosphodiesterase 1, anticorps sphingomyelin phosphodiesterase 1, acid lysosomal, anticorps sphingomyelin phosphodiesterase, anticorps SMPD1, anticorps Smpd1, anticorps LOC5578088
- Sujet
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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.
Alias Symbols: ASM, NPD, ASMASE
Protein Size: 171 - Poids moléculaire
- 18 kDa
- ID gène
- 6609
- NCBI Accession
- NM_000543, NP_000534
- UniProt
- P17405
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