NIPA1 Antikörper (AA 161-260) (HRP)
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- Target Alle NIPA1 Antikörper anzeigen
- NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))
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Bindungsspezifität
- AA 161-260
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser NIPA1 Antikörper ist konjugiert mit HRP
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Applikation
- ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Kreuzreaktivität
- Human
- Homologie
- Mouse,Rat,Dog
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human NIPA1
- Isotyp
- IgG
- Top Product
- Discover our top product NIPA1 Primärantikörper
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- Applikationshinweise
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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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Haltbarkeit
- 12 months
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- Target
- NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))
- Andere Bezeichnung
- NIPA1 (NIPA1 Produkte)
- Synonyme
- FSP3 antikoerper, SPG6 antikoerper, 1110027G09Rik antikoerper, A830014A18Rik antikoerper, Spg6 antikoerper, non imprinted in Prader-Willi/Angelman syndrome 1 antikoerper, non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human) antikoerper, NIPA1 antikoerper, Nipa1 antikoerper
- Hintergrund
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Synonyms: FSP 3, FSP3, Magnesium transporter NIPA1, MGC102724, MGC35570, NIPA 1, NIPA1, NIPA1_HUMAN, Non imprinted in Prader Willi/Angelman syndrome region protein 1, Non-imprinted in Prader-Willi/Angelman syndrome region protein 1, Spastic paraplegia 6 (autosomal dominant), Spastic paraplegia 6 protein, SPG 6, SPG6.
Background: This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6. [provided by RefSeq, Nov 2008]
- Gen-ID
- 123606
- UniProt
- Q7RTP0
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