Arylsulfatase B anticorps (AA 404-533)
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- Antigène Voir toutes Arylsulfatase B (ARSB) Anticorps
- Arylsulfatase B (ARSB)
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Épitope
- AA 404-533
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp Arylsulfatase B est non-conjugé
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Application
- Western Blotting (WB)
- Fonction
- ARSB Rabbit pAb
- Séquence
- PCPRNSMAPA KDDSSLPEYS AFNTSVHAAI RHGNWKLLTG YPGCGYWFPP PSQYNVSEIP SSDPPTKTLW LFDIDRDPEE RHDLSREYPH IVTKLLSRLQ FYHKHSVPVY FPAQDPRCDP KATGVWGPWM
- Réactivité croisée
- Humain
- Attributs du produit
- Polyclonal Antibodies
- Purification
- Affinity purification
- Immunogène
- Recombinant fusion protein containing a sequence corresponding to amino acids 404-533 of human ARSB (NP_000037.2).
- Isotype
- IgG
- Top Product
- Discover our top product ARSB Anticorps primaire
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- Indications d'application
- WB,1:500 - 1:2000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 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.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- Arylsulfatase B (ARSB)
- Autre désignation
- ARSB (ARSB Produits)
- Synonymes
- anticorps ASB, anticorps G4S, anticorps MPS6, anticorps 1110007C02Rik, anticorps AI480648, anticorps As-1, anticorps As-1r, anticorps As-1s, anticorps As-1t, anticorps As1, anticorps As1-r, anticorps As1-s, anticorps As1-t, anticorps Asr-1, anticorps Ast-1, anticorps ARSB, anticorps arylsulfatase B, anticorps arylsulfatase, anticorps arylsulfatase b, anticorps ARSB, anticorps Arsb, anticorps RB348, anticorps LOC5566067, anticorps CpipJ_CPIJ011047, anticorps VDBG_03275, anticorps arsb, anticorps LOC5579667
- Sujet
- Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targeted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.,ARSB,ASB,G4S,MPS6,Cancer,Signal Transduction,Cell Biology & Developmental Biology,Autophagy,Endocrine & Metabolism,ARSB
- Poids moléculaire
- 45kDa/59kDa
- ID gène
- 411
- UniProt
- P15848
- Pathways
- Glycosaminoglycan Metabolic Process
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