SPG7 Recombinant Rabbit Monoclonal Antibody (HL2236), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | FEMA550450-Each-of-1 | In Stock | ₹ 41,385.00 |
FEMA550450 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 41,385.00
GST (18%): ₹ 7,449.30
Total Price: ₹ 48,834.30
Antigen
SPG7
Classification
Recombinant Monoclonal
Concentration
1 mg/mL
Formulation
PBS with no preservative
Gene Accession No.
Q3ULF4, Q7TT47, Q9UQ90
Gene Symbols
SPG7
Immunogen
Recombinant fragmemt of human SPG7.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Form
Liquid
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Clone
HL2236
Conjugate
Unconjugated
Gene
SPG7
Gene Alias
AI452278, AU015315, CAR, cell adhesion regulator, cell matrix adhesion regulator, CMAR, paraplegin, paraplegin, isoform 1, PGN, spastic paraplegia 7 (pure and complicated autosomal recessive), spastic paraplegia 7 homolog (human), spastic paraplegia 7 protein, SPG5C, SPG7, SPG7 matrix AAA peptidase subunit, paraplegin, SPG7, paraplegin matrix AAA peptidase subunit
Host Species
Rabbit
Purification Method
Protein A
Regulatory Status
RUO
Gene ID (Entrez)
234847, 353231, 6687
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Isotype
IgG
Related Products
Description
- Description This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family
- Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis
- Mutations in this gene cause autosomal recessive spastic paraplegia 7
- Two transcript variants encoding distinct isoforms have been identified.