NIPA1 anticorps (C-Term)
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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
- C-Term
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Reactivité
- Humain, Souris, Chien, Cobaye, Cheval, Rat, Boeuf (Vache)
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp NIPA1 est non-conjugé
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Application
- Western Blotting (WB)
- Séquence
- FREWSNVGLV DFLGMACGFT TVSVGIVLIQ VFKEFNFNLG EMNKSNMKTD
- Homologie
- Cow: 93%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rat: 100%
- Attributs du produit
- This is a rabbit polyclonal antibody against NIPA1. It was validated on Western Blot.
- Purification
- Affinity Purified
- Top Product
- Discover our top product NIPA1 Anticorps primaire
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- Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator.
- Commentaires
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Antigen size: 254 AA
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- Lot specific
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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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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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.
Alias Symbols: FSP3, MGC102724, MGC35570, SPG6
Protein Size: 254 - Poids moléculaire
- 27 kDa
- ID gène
- 123606
- NCBI Accession
- NM_001142275, NP_001135747
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