SMPD1 anticorps (Middle Region)

N° du produit ABIN2776372

Détail du produit anti-SMPD1 anticorps

Antigène: SMPD1 (Sphingomyelin phosphodiesterase 1, Acid Lysosomal (SMPD1))

Épitope: Middle Region

Reactivité: Humain, Souris, Rat, Boeuf (Vache), Mouton, Lapin, Chien, Cheval, Cobaye

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SMPD1 est non-conjugé

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

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

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.

Détails sur SMPD1

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: 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