Arylsulfatase B Antikörper (AA 235-266)
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- Target Alle Arylsulfatase B (ARSB) Antikörper anzeigen
- Arylsulfatase B (ARSB)
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Bindungsspezifität
- AA 235-266
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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)
- Aufreinigung
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogen
- This ARSB antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 235-266 amino acids from the Central region of human ARSB.
- Klon
- RB18352
- Isotyp
- Ig Fraction
- Top Product
- Discover our top product ARSB Primärantikörper
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- Applikationshinweise
- WB: 1:1000. WB: 1:1000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- Purified polyclonal antibody supplied in 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.
- Lagerung
- 4 °C,-20 °C
- Informationen zur Lagerung
- Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
- Haltbarkeit
- 6 months
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- Target
- Arylsulfatase B (ARSB)
- Andere Bezeichnung
- ARSB (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.
- Molekulargewicht
- 59687
- Gen-ID
- 411
- NCBI Accession
- NP_000037, NP_942002
- UniProt
- P15848
- Pathways
- Glycosaminoglycan Metabolic Process
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