Arylsulfatase B Antikörper (Middle Region)
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- Target Alle Arylsulfatase B (ARSB) Antikörper anzeigen
- Arylsulfatase B (ARSB)
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Bindungsspezifität
- Middle Region
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser Arylsulfatase B Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Enzyme Immunoassay (EIA)
- Spezifität
- This antibody reacts to Arylsulfatase B.
- Aufreinigung
- Affinity chromatography on Protein A
- Immunogen
- KLH conjugated synthetic peptide selected from the Center region of human ARSB
- Top Product
- Discover our top product ARSB Primärantikörper
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- Applikationshinweise
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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. - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 0.25 mg/mL
- Buffer
- PBS with 0.09 % (W/V) sodium azide
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handhabung
- Avoid repeated freezing and thawing.
- Lagerung
- 4 °C/-20 °C
- Informationen zur Lagerung
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- Target
- Arylsulfatase B (ARSB)
- Andere Bezeichnung
- Arylsulfatase B (ARSB Produkte)
- Synonyme
- ASB antikoerper, G4S antikoerper, MPS6 antikoerper, 1110007C02Rik antikoerper, AI480648 antikoerper, As-1 antikoerper, As-1r antikoerper, As-1s antikoerper, As-1t antikoerper, As1 antikoerper, As1-r antikoerper, As1-s antikoerper, As1-t antikoerper, Asr-1 antikoerper, Ast-1 antikoerper, ARSB antikoerper, arylsulfatase B antikoerper, arylsulfatase antikoerper, arylsulfatase b antikoerper, ARSB antikoerper, Arsb antikoerper, RB348 antikoerper, LOC5566067 antikoerper, CpipJ_CPIJ011047 antikoerper, VDBG_03275 antikoerper, arsb antikoerper, LOC5579667 antikoerper
- Hintergrund
- 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
- Gen-ID
- 411
- NCBI Accession
- NP_000037
- UniProt
- P15848
- Pathways
- Glycosaminoglycan Metabolic Process
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