NIPA1 Antikörper (AA 161-260) (Alexa Fluor 555)

Produktnummer ABIN6978524

Produktdetails anti-NIPA1 Antikörper (Alexa Fluor 555)

Target: NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))

Bindungsspezifität: AA 161-260

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NIPA1 Antikörper ist konjugiert mit Alexa Fluor 555

Applikation: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Kreuzreaktivität: Human

Homologie: Mouse,Rat,Dog

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human NIPA1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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

Details zu NIPA1

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:

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