PEX19 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA522129-Each-of-1 | In Stock | ₹ 52,510.00 |
PIPA522129 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 52,510.00
GST (18%): ₹ 9,451.80
Total Price: ₹ 61,961.80
Antigen
PEX19
Classification
Polyclonal
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
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
19298, 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
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Concentration
1.01 mg/mL
Formulation
PBS with 20% glycerol and 0.025% ProClin 300; pH 7
Gene Accession No.
P40855, Q8VCI5, Q9QYU1
Gene Symbols
PEX19
Immunogen
Recombinant fragment corresponding to a region within amino acids 1 and 299 of PEX19 (Uniprot ID#P40855)
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Recommended positive controls: Jurkat, Raji, NCI-H929, K562, THP-1, HL-60, mouse liver, PC-12, Rat-2
- 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).