Peroxisomal Biogenesis Factor 12 (PEX12) (Middle Region) Peptid
PEX12
Reaktivität: Human
Wirt: Synthetic
WB
Produktnummer ABIN5518157
Kurzübersicht für Peroxisomal Biogenesis Factor 12 (PEX12) (Middle Region) Peptid (ABIN5518157)
Target
PEX12
(Peroxisomal Biogenesis Factor 12 (PEX12))
Spezies
Human
Quelle
Synthetic
Applikation
Western Blotting (WB)
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Protein Region
- Middle Region
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Sequenz
- SIMFLVLLPY LKVKLEKLVS SLREEDEYSI HPPSSRWKRF YRAFLAAYPF
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Lyophilized
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Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))
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Hintergrund
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This gene belongs to the peroxin-12 family. 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. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 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 are a cause of Zellweger syndrome (ZWS).
Alias Symbols: PAF-3, PBD3A
Protein Size: 167 -
Gen-ID
- 5193
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NCBI Accession
- NM_000286, NP_000277
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UniProt
- O00623
Target
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