PLP1 Monoclonal Antibody (plpc 1), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA190652-Each-of-1 | In Stock | ₹ 53,667.00 |
PIMA190652 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 53,667.00
GST (18%): ₹ 9,660.06
Total Price: ₹ 63,327.06
Antigen
PLP1
Classification
Monoclonal
Concentration
1 mg/mL
Formulation
PBS with 0.09% sodium azide
Gene Accession No.
P04116, P60201, P60202
Gene Symbols
PLP1
Immunogen
Synthetic peptide-amino acids CGRGTKF corresponding to C terminal region of myelin proteolipid protein.
Quantity
50 μg
Primary or Secondary
Primary
Target Species
Bovine, Human, Mouse, Mouse, Rat
Product Type
Antibody
Isotype
IgG2a
Applications
Flow Cytometry, Immunocytochemistry, Immunohistochemistry (Frozen), Immunohistochemistry (Paraffin), Western Blot
Clone
plpc 1
Conjugate
Unconjugated
Gene
PLP1
Gene Alias
DM20; GPM6C; HLD1; jimpy; jp; lipophilin; lipophilin (aa 129 to 276); major myelin proteolipid protein; MMPL; msd; Myelin proteolipid protein; myelin synthesis deficiency; PLP; PLP/DM20; Plp1; PMD; proteolipid; proteolipid protein; proteolipid protein (myelin) 1; Proteolipid protein (Pelizaeus-Merzbacher disease spastic paraplegia 2 uncomplicated); Proteolipid protein (Pelizaeus-Merzbacher disease, spastic paraplegia 2, uncomplicated); proteolipid protein 1; proteolipid protein 1 (Pelizaeus-Merzbacher disease, spastic paraplegia 2, uncomplicated); proteolipid protein, lipophilin; rsh; rump shaker; SPG2
Host Species
Mouse
Purification Method
Protein A
Regulatory Status
RUO
Gene ID (Entrez)
18823, 281410, 5354
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
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- PLP1 is a transmembrane proteolipid protein that is the predominant myelin protein present in the central nervous system
- It may play a role in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival
- Mutations in this gene cause X-linked Pelizaeus-Merzbacher disease and spastic paraplegia type 2
- Alternatively spliced transcript variants encoding distinct isoforms or having different 5' UTRs, have been identified for this gene.This gene encodes a transmembrane proteolipid protein that is the predominant myelin protein present in the central nervous system
- It may play a role in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival
- Mutations in this gene cause X-linked Pelizaeus-Merzbacher disease and spastic paraplegia type 2
- Alternatively spliced transcript variants encoding distinct isoforms or having different 5' UTRs, have been identified for this gene.