IMPAD1 Antikörper (AA 81-180) (Biotin)
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- Target Alle IMPAD1 Antikörper anzeigen
- IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))
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Bindungsspezifität
- AA 81-180
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser IMPAD1 Antikörper ist konjugiert mit Biotin
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Applikation
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Homologie
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human IMPAD1
- Isotyp
- IgG
- Top Product
- Discover our top product IMPAD1 Primärantikörper
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- Applikationshinweise
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C for 12 months.
- Haltbarkeit
- 12 months
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- Target
- IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))
- Andere Bezeichnung
- IMPAD1 (IMPAD1 Produkte)
- Hintergrund
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Synonyms: IMP 3, IMPA3, IMPase 3, Inositol monophosphatase domain containing protein 1, Myo inositol monophosphatase A3.
Background: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.
- Gen-ID
- 54928
- Pathways
- Glycosaminoglycan Metabolic Process
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