NPAP1 anticorps (AA 800-850)
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- Antigène Voir toutes NPAP1 Anticorps
- NPAP1 (Nuclear Pore Associated Protein 1 (NPAP1))
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Épitope
- AA 800-850
- Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp NPAP1 est non-conjugé
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Réactivité croisée
- Humain
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human NPAP1
- Isotype
- IgG
- Top Product
- Discover our top product NPAP1 Anticorps primaire
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- Indications d'application
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- Stockage commentaire
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- NPAP1 (Nuclear Pore Associated Protein 1 (NPAP1))
- Autre désignation
- NPAP1 (NPAP1 Produits)
- Synonymes
- anticorps C15orf2, anticorps nuclear pore associated protein 1, anticorps NPAP1
- Sujet
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Synonyms: NPAP1, NPAP 1, NPAP-1, Nuclear pore associated protein 1, NPAP1_HUMAN, C15orf2.
Background: This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome. May be involved in spermatogenesis.
- ID gène
- 23742
- UniProt
- Q9NZP6
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