Peroxisomal Biogenesis Factor 12 (PEX12) (Middle Region) Peptide
PEX12
Reactivity: Human
Host: Synthetic
WB
Catalog No. ABIN5518157
Quick Overview for Peroxisomal Biogenesis Factor 12 (PEX12) (Middle Region) Peptide (ABIN5518157)
Target
PEX12
(Peroxisomal Biogenesis Factor 12 (PEX12))
Origin
Human
Source
Synthetic
Application
Western Blotting (WB)
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Protein Region
- Middle Region
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Sequence
- SIMFLVLLPY LKVKLEKLVS SLREEDEYSI HPPSSRWKRF YRAFLAAYPF
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Storage
- -20 °C
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Storage Comment
- 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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Background
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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 -
Gene ID
- 5193
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NCBI Accession
- NM_000286, NP_000277
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UniProt
- O00623
Target
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