PEX7 anticorps (AA 180-260)
Aperçu rapide pour PEX7 anticorps (AA 180-260) (ABIN7223122)
Antigène
Voir toutes PEX7 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 180-260
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Fonction
- Peroxin 7 Polyclonal Antibody
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Specificité
- Peroxin 7 Polyclonal Antibody detects endogenous levels of Peroxin 7 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogène
- Synthesized peptide derived from the Internal region of human Peroxin 7 at AA range: 180-260
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Isotype
- IgG
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Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:40000). Not yet tested in other applications.
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Commentaires
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- PEX7 (Peroxisomal Biogenesis Factor 7 (PEX7))
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Autre désignation
- Peroxin 7
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Sujet
- Rabbit Anti-Peroxin 7 Polyclonal Antibody,PEX7, PTS2R, Peroxisomal targeting signal 2 receptor, PTS2 receptor, Peroxin-7,PEX7 (peroxisomal biogenesis factor 7) encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2). Defects in PEX7 cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function. There are at least 14 complementation groups for PBDs, with more than one phenotype being observed in cases falling into particular 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 have been associated with PBD complementation group 11 (PBD-CG11) disorders, rhizomelic chondrodysplasia punctata type 1 (RCDP1), and Refsum disease (RD).,Peroxisomal targeting signal 2 receptor
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Poids moléculaire
- observerd band 40kDa
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ID gène
- 5191
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UniProt
- O00628
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Pathways
- Monocarboxylic Acid Catabolic Process
Antigène
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