PEX19 Monoclonal Antibody (GT533), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA517281-Each-of-1 | In Stock | ₹ 47,481.50 |
PIMA517281 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 47,481.50
GST (18%): ₹ 8,546.67
Total Price: ₹ 56,028.17
Antigen
PEX19
Classification
Monoclonal
Concentration
1.17 mg/mL
Formulation
PBS with no preservative
Gene Accession No.
P40855, Q9QYU1
Gene Symbols
PEX19
Immunogen
Recombinant fragment contains a sequence corresponding to a region within amino acids 15 and 299 of PEX19
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Rat
Product Type
Antibody
Isotype
IgG2b
Applications
Flow Cytometry, Immunocytochemistry, Western Blot
Clone
GT533
Conjugate
Unconjugated
Gene
PEX19
Gene Alias
33 kDa housekeeping protein; D1S2223E; HK33; housekeeping gene, 33kD; OK/SW-cl.22; PBD12A; peroxin-19; Peroxisomal biogenesis factor 19; peroxisomal farnesylated protein; peroxisome biogenesis factor 19; Pex19; PMP1; PMPI; PxF; PXMP1
Host Species
Mouse
Purification Method
Protein G
Regulatory Status
RUO
Gene ID (Entrez)
289233, 5824
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Related Products
Description
- Recommended positive controls: Jurkat, Raji, K562, THP-1, NCI-H929, PC-12, Rat2
- Predicted reactivity: Mouse (91%), Rat (93%), Bovine (95%)
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- This gene is necessary for early peroxisomal biogenesis
- It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs)
- 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 Zellweger syndrome (ZWS).