PEX1 Antikörper (AA 1210-1290)
Kurzübersicht für PEX1 Antikörper (AA 1210-1290) (ABIN7223120)
Target
Alle PEX1 Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- AA 1210-1290
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Verwendungszweck
- Peroxin 1 Polyclonal Antibody
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Spezifität
- Peroxin 1 Polyclonal Antibody detects endogenous levels of Peroxin 1 protein.
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Aufreinigung
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from the C-terminal region of human Peroxin 1 at AA range: 1210-1290
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Isotyp
- IgG
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Applikationshinweise
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: IHC-P (1:100-1:300), ELISA (1:10000). Not yet tested in other applications.
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Kommentare
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Primary Antibody
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- 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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- PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))
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Andere Bezeichnung
- Peroxin 1
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Hintergrund
- Rabbit Anti-Peroxin 1 Polyclonal Antibody,PEX1, Peroxisome biogenesis factor 1, Peroxin-1, Peroxisome biogenesis disorder protein 1,PEX1 (peroxisomal biogenesis factor 1) encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in PEX1 have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene.,Peroxisome biogenesis factor 1
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Gen-ID
- 5189
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UniProt
- O43933
Target
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