ALDH4A1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA529119-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA529119 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
ALDH4A1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
Aldh4a1
Gene Alias
A930035F14Rik; Ahd1; Ahd-1; aldehyde dehydrogenase 4 family member A1; aldehyde dehydrogenase 4 family, member A1; aldehyde dehydrogenase 4A1; aldehyde dehydrogenase family 4 member A1; ALDH4; aldh4a1; Aldh5a1; delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial; E330022C09; L-glutamate gamma-semialdehyde dehydrogenase; mitochondrial delta-1-pyrroline 5-carboxylate dehydrogenase; P5C dehydrogenase; P5cd; P5CDh; P5cdhl; P5cdhs; RP11-128M10.1; similar to aldehyde dehydrogenase 4 family, member A1; Ssdh1; zgc:63592
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
8659
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
0.1M tris glycine with 10% glycerol and 0.01% thimerosal; pH 7
Gene Accession No.
P30038
Gene Symbols
Aldh4a1
Immunogen
Recombinant fragment corresponding to a region within amino acids 241 and 529 of Human ALDH4A1
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Recommended positive controls: HepG2
- Predicted reactivity: Mouse (90%), Rat (90%), Pig (91%), Bovine (88%)
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- ALDH4A1 belongs to the aldehyde dehydrogenase family of proteins
- This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate
- Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline.