PEX12 polyclonal (Center), anti-human
€0.00
In stock
SKU
AC-AP9604c
Catalog Number: AC-AP9604c
Size: 80 µl, 400 µl
Isotype: Rabbit IgG
Clone Name: RB22647
Applications: WB
Datasheet
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Size: 80 µl, 400 µl
Isotype: Rabbit IgG
Clone Name: RB22647
Applications: WB
Datasheet
Request Information
Background:
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.
Other Names:
Peroxisome assembly protein 12, Peroxin-12, Peroxisome assembly factor 3, PAF-3, PEX12, PAF3
Target/Specificity:
This PEX12 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 131-158 amino acids from the Central region of human PEX12.
Antigen Region:
131-158
Antigen Type: Synthetic Peptide
Gene Name: PEX12 {ECO:0000303|PubMed:9090384, ECO:0000312|HGNC:HGNC:8854}
Gene ID: 5193
Primary Accession: O00623
NCBI Accession: NP_000277.1
Other Accession: Q8VC48; A4FUD4
Format: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
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.
Other Names:
Peroxisome assembly protein 12, Peroxin-12, Peroxisome assembly factor 3, PAF-3, PEX12, PAF3
Target/Specificity:
This PEX12 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 131-158 amino acids from the Central region of human PEX12.
Antigen Region:
131-158
Antigen Type: Synthetic Peptide
Gene Name: PEX12 {ECO:0000303|PubMed:9090384, ECO:0000312|HGNC:HGNC:8854}
Gene ID: 5193
Primary Accession: O00623
NCBI Accession: NP_000277.1
Other Accession: Q8VC48; A4FUD4
Format: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
| Is Featured? | No |
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