AGPS Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA576591-Each-of-1 | In Stock | ₹ 49,528.50 |
PIPA576591 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 49,528.50
GST (18%): ₹ 8,915.13
Total Price: ₹ 58,443.63
Antigen
AGPS
Classification
Polyclonal
Conjugate
Unconjugated
Gene
AGPS
Gene Alias
5832437L22; 9930035G10Rik; AAG5; Adaps; Adap-s; ADAS; Adhaps; ADPS; Ads; Aging-associated gene 5 protein; aging-associated protein 5; AGPS; ALDHPSY; alkyl-DHAP synthase; alkyldihydroxyacetone phosphate synthase; alkyl-dihydroxyacetonephosphate synthase; alkyldihydroxyacetonephosphate synthase, peroxisomal; alkylglycerone phosphate synthase; alkylglycerone phosphate synthase-like; alkylglycerone-phosphate synthase; AW123847; bs2; RCDP3
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
228061, 8540
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Western Blot
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide; pH 7.2
Gene Accession No.
O00116, Q8C0I1
Gene Symbols
AGPS
Immunogen
Recombinant protein of human AGPS
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse
Product Type
Antibody
Isotype
IgG
Related Products
Description
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE)
- This gene is a member of the FAD-binding oxidoreductase/transferase type 4 family
- It encodes a protein that catalyzes the second step of ether lipid biosynthesis in which acyl-dihydroxyacetonephosphate (DHAP) is converted to alkyl-DHAP by the addition of a long chain alcohol and the removal of a long-chain acid anion
- The protein is localized to the inner aspect of the peroxisomal membrane and requires FAD as a cofactor
- Mutations in this gene have been associated with rhizomelic chondrodysplasia punctata, type 3 and Zellweger syndrome.