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)
- Synonyme
- IMP 3 antikoerper, RGD1306455 antikoerper, gPAPP antikoerper, impa3 antikoerper, 1110001C20Rik antikoerper, AA408880 antikoerper, AI451589 antikoerper, AL022796 antikoerper, B230207P20 antikoerper, Jaws antikoerper, GPAPP antikoerper, IMP-3 antikoerper, IMPA3 antikoerper, IMPase 3 antikoerper, zgc:123256 antikoerper, inositol monophosphatase domain containing 1 antikoerper, inositol monophosphatase domain containing 1 S homeolog antikoerper, Impad1 antikoerper, impad1.S antikoerper, IMPAD1 antikoerper, impad1 antikoerper
- 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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