Arylsulfatase B anticorps (C-Term)
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- Antigène Voir toutes Arylsulfatase B (ARSB) Anticorps
- Arylsulfatase B (ARSB)
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Épitope
- C-Term
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Reactivité
- Humain, Souris, Rat
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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), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)
- Specificité
- ARSB antibody is human, mouse and rat reactive. At least two isoforms of ARSB are known to exist, this antibody only recognizes the longest isoform.
- Purification
- ARSB Antibody is affinity chromatography purified via peptide column.
- Immunogène
- ARSB antibody was raised against a 16 amino acid peptide near the carboxy terminus of human ARSB
- Isotype
- IgG
- Top Product
- Discover our top product ARSB Anticorps primaire
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- Indications d'application
- ARSB antibody can be used for detection of ARSB by Western blot at 1 - 2 μg/mL.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- PBS containing 0.02 % 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.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- Can be stored at 4 °C for three months and -20 °C, stable for up to one year.
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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
- Aryl sulfatase B (ARSB) forms a homodimer that hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate (1). ARSB localizes to the lysozyme as well as to the extracellular matrix (2). Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B (3), and can be treated with exogenous ARSB (4).
- Poids moléculaire
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Predicted: 59 kDa
Observed: 57kDa - ID gène
- 411
- NCBI Accession
- NP_000037
- UniProt
- P15848
- Pathways
- Glycosaminoglycan Metabolic Process
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