ALDH4A1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA582246-Each-of-1 | In Stock | ₹ 52,332.00 |
PIPA582246 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 52,332.00
GST (18%): ₹ 9,419.76
Total Price: ₹ 61,751.76
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
Anitgen affinity chromatography, 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
Immunohistochemistry, Western Blot
Concentration
0.1 mg/mL
Formulation
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2
Gene Accession No.
P30038
Gene Symbols
Aldh4a1
Immunogen
Recombinant protein corresponding to Human ALDH4A1
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Immunogen sequence: KSLLNKAIEA ALAARKEWDL KPIADRAQIF LKAADMLSGP RRAEILAKTM VGQGKTVIQA EIDAAAELID FFRFNAKYAV ELEGQQPISV PPSTNSTVYR GLE 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.