Arylsulfatase B anticorps (Middle Region)
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- Antigène Voir toutes Arylsulfatase B (ARSB) Anticorps
- Arylsulfatase B (ARSB)
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Épitope
- Middle Region
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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), Enzyme Immunoassay (EIA)
- Specificité
- This antibody reacts to Arylsulfatase B.
- Purification
- Affinity chromatography on Protein A
- Immunogène
- KLH conjugated synthetic peptide selected from the Center region of human ARSB
- Top Product
- Discover our top product ARSB Anticorps primaire
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- Indications d'application
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ELISA: 1/1,000. Western blotting: 1/100 - 1/500.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user. - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.25 mg/mL
- Buffer
- PBS with 0.09 % (W/V) sodium azide
- 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 repeated freezing and thawing.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- Antigène
- Arylsulfatase B (ARSB)
- Autre désignation
- Arylsulfatase B (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
- ARSB 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 targetted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B.Synonyms: ARSB, ASB, G4S, N-acetylgalactosamine-4-sulfatase
- ID gène
- 411
- NCBI Accession
- NP_000037
- UniProt
- P15848
- Pathways
- Glycosaminoglycan Metabolic Process
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