PEX14 anticorps (AA 151-250) (Biotin)
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- Antigène Voir toutes PEX14 Anticorps
- PEX14 (Peroxisomal Biogenesis Factor 14 (PEX14))
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Épitope
- AA 151-250
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Reactivité
- Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp PEX14 est conjugé à/à la Biotin
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Application
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Réactivité croisée
- Rat
- Homologie
- Human,Mouse,Dog,Cow,Sheep,Horse,Chicken,Rabbit
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human PEX14
- Isotype
- IgG
- Top Product
- Discover our top product PEX14 Anticorps primaire
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- Indications d'application
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IHC-P 1:200-400
IHC-F 1:100-500 - 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 for 12 months.
- Date de péremption
- 12 months
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- Antigène
- PEX14 (Peroxisomal Biogenesis Factor 14 (PEX14))
- Autre désignation
- PEX14 (PEX14 Produits)
- Sujet
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Synonyms: dJ734G22.2, NAPP2, NF E2 associated polypeptide 2, Peroxin 14, Peroxin-14, Peroxisomal biogenesis factor 14, Peroxisomal membrane anchor protein PEX14, Peroxisomal membrane anchor protein Pex14p, Peroxisomal membrane protein PEX14, pex14, PEX14_HUMAN, Pex14p, PTS1 receptor docking protein, PTS1 receptor-docking protein.
Background: This gene encodes an essential component of the peroxisomal import machinery. The protein is integrated into peroxisome membranes with its C-terminus exposed to the cytosol, and interacts with the cytosolic receptor for proteins containing a PTS1 peroxisomal targeting signal. The protein also functions as a transcriptional corepressor and interacts with a histone deacetylase. A mutation in this gene results in one form of Zellweger syndrome. [provided by RefSeq, Jul 2008]
- ID gène
- 5195
- UniProt
- O75381
- Pathways
- Maintenance of Protein Location
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