PEX19 anticorps
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- Antigène Voir toutes PEX19 Anticorps
- PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Monoclonal
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Conjugué
- Cet anticorp PEX19 est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
- Réactivité croisée
- Humain
- Purification
- Purified by Protein A.
- Immunogène
- Synthetic peptide within N-terminal Human PEX19.
- Clone
- 9H3
- Isotype
- IgG
- Top Product
- Discover our top product PEX19 Anticorps primaire
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- Indications d'application
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WB 1:300-5000
FCM 1:20-100
IHC-P 1:200-400 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 1xTBS ( pH 7.4), 1 % BSA, 40 %Glycerol and 0.05 % Sodium Azide.
- 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
- PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))
- Autre désignation
- PEX19 (PEX19 Produits)
- Synonymes
- anticorps BEST:GH03076, anticorps CG5325, anticorps DmelPex19, anticorps Dmel\\CG5325, anticorps D1S2223E, anticorps HK33, anticorps PBD12A, anticorps PMP1, anticorps PMPI, anticorps PXF, anticorps PXMP1, anticorps Pxf, anticorps PxF, anticorps Peroxin-19, anticorps Peroxin 19, anticorps Peroxisomal farnesylated protein, anticorps peroxisomal biogenesis factor 19, anticorps Pex19, anticorps Bm1_19905, anticorps PEX19
- Sujet
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Synonyms: 33 kDa housekeeping protein antibody, D1S2223E antibody, HK33 antibody, Housekeeping gene 33kD antibody, OK/SW-cl.22 antibody, PBD12A antibody, Peroxin 19 antibody, Peroxin-19 antibody, Peroxisomal biogenesis factor 19 antibody, Peroxisomal farnesylated protein antibody, PEX19 antibody, PEX19_HUMAN antibody, PMP1 antibody, PMPI antibody, PXF antibody, PXMP1 antibody
Background: This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]
- ID gène
- 5824
- UniProt
- P40855
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