NIPA1 anticorps (AA 161-260) (AbBy Fluor® 594)
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- Antigène Voir toutes NIPA1 Anticorps
- NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))
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Épitope
- AA 161-260
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp NIPA1 est conjugé à/à la AbBy Fluor® 594
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Application
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Humain
- Homologie
- Mouse,Rat,Dog
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human NIPA1
- Isotype
- IgG
- Top Product
- Discover our top product NIPA1 Anticorps primaire
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- Indications d'application
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))
- Autre désignation
- NIPA1 (NIPA1 Produits)
- Synonymes
- anticorps FSP3, anticorps SPG6, anticorps 1110027G09Rik, anticorps A830014A18Rik, anticorps Spg6, anticorps non imprinted in Prader-Willi/Angelman syndrome 1, anticorps non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human), anticorps NIPA1, anticorps Nipa1
- Sujet
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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]
- ID gène
- 123606
- UniProt
- Q7RTP0
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