Arylsulfatase E Antikörper (AA 520-589)
Kurzübersicht für Arylsulfatase E Antikörper (AA 520-589) (ABIN7265688)
Target
Alle Arylsulfatase E (ARSE) Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- AA 520-589
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Verwendungszweck
- ARSE Rabbit pAb
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Sequenz
- PSETHILTPA SEPVFYQVME RVQQAVWEHQ RTLSPVPLQL DRLGNIWRPW LQPCCGPFPL CWCLREDDPQ
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Kreuzreaktivität
- Maus, Ratte
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Produktmerkmale
- Polyclonal Antibodies
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Aufreinigung
- Affinity purification
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Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 520-589 of human ARSE (NP_000038.2).
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Isotyp
- IgG
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anti-Arylsulfatase E (ARSE) (AA 352-494) antibody
ARSE Reaktivität: Human ELISA, IHC, IF Wirt: Kaninchen Polyclonal unconjugated
anti-Arylsulfatase E (ARSE) (Internal Region) antibodyARSE Reaktivität: Human ELISA, WB, IF, ICC Wirt: Kaninchen Polyclonal unconjugated
anti-Arylsulfatase E (ARSE) (AA 490-589) antibodyARSE Reaktivität: Human ELISA, WB Wirt: Maus Polyclonal unconjugated
anti-Arylsulfatase E (ARSE) (AA 504-553) antibodyARSE Reaktivität: Human WB, IHC, IHC (p) Wirt: Kaninchen Polyclonal unconjugated
anti-Arylsulfatase E (ARSE) (C-Term) antibodyARSE Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
anti-Arylsulfatase E (ARSE) (Internal Region) antibodyARSE Reaktivität: Human ELISA, WB Wirt: Kaninchen Polyclonal unconjugated
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Applikationshinweise
- WB,1:500 - 1:2000
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Arylsulfatase E (ARSE)
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Andere Bezeichnung
- ARSE
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Hintergrund
- Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome.,ARSE,ASE,CDPX,CDPX1,CDPXR,Cell Biology & Developmental Biology,Extracellular Matrix,Bone,ARSE
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Molekulargewicht
- 65kDa
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Gen-ID
- 415
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UniProt
- P51690
Target
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