Recombinant Human ALDH3A2 Protein, Myc/DDK-tagged, C13 and N15-labeled
Cat.No. : | ALDH3A2-3221H |
Product Overview : | ALDH3A2 MS Standard C13 and N15-labeled recombinant protein (NP_000373) with a C-terminal MYC/DDK tag, was expressed in HEK293 cells. |
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Description : | Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This gene product catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acid. Mutations in the gene cause Sjogren-Larsson syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. |
Source : | HEK293 |
Species : | Human |
Tag : | Myc/DDK |
Molecular Mass : | 54.7 kDa |
AA Sequence : | MELEVRRVRQAFLSGRSRPLRFRLQ QLEALRRMVQEREKDILTAIAADLC KSEFNVYSQEVITVLGEIDFMLENL PEWVTAKPVKKNVLTMLDEAYIQPQ PLGVVLIIGAWNYPFVLTIQPLIGA IAAGNAVIIKPSELSENTAKILAKL LPQYLDQDLYIVINGGVEETTELLK QRFDHIFYTGNTAVGKIVMEAAAKH LTPVTLELGGKSPCYIDKDCDLDIV CRRITWGKYMNCGQTCIAPDYILCE ASLQNQIVWKIKETVKEFYGENIKE SPDYERIINLRHFKRILSLLEGQKI AFGGETDEATRYIAPTVLTDVDPKT KVMQEEIFGPILPIVPVKNVDEAIN FINEREKPLALYVFSHNHKLIKRMI DETSSGGVTGNDVIMHFTLNSFPFG GVGSSGMGAYHGKHSFDTFSHQRPC LLKSLKREGANKLRYPPNSQSKVDW GKFFLLKRFNKEKLGLLLLTFLGIV AAVLVKAEYYTRTRPLEQKLISEED LAANDILDYKDDDDKV |
Purity : | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Stability : | Stable for 3 months from receipt of products under proper storage and handling conditions. |
Storage : | Store at -80 centigrade. Avoid repeated freeze-thaw cycles. |
Concentration : | 50 μg/mL as determined by BCA |
Storage Buffer : | 100 mM glycine, 25 mM Tris-HCl, pH 7.3. |
Gene Name : | ALDH3A2 aldehyde dehydrogenase 3 family member A2 [ Homo sapiens (human) ] |
Official Symbol : | ALDH3A2 |
Synonyms : | ALDH3A2; aldehyde dehydrogenase 3 family, member A2; ALDH10, SLS; fatty aldehyde dehydrogenase; FALDH; aldehyde dehydrogenase 10; microsomal aldehyde dehydrogenase; aldehyde dehydrogenase family 3 member A2; SLS; ALDH10; FLJ20851; DKFZp686E23276; |
Gene ID : | 224 |
mRNA Refseq : | NM_000382 |
Protein Refseq : | NP_000373 |
MIM : | 609523 |
UniProt ID : | P51648 |
Products Types
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◆ Lysates | ||
ALDH3A2-8917HCL | Recombinant Human ALDH3A2 293 Cell Lysate | +Inquiry |
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For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (13)
Ask a questionCurrently, there are no specific drugs or treatments designed to target ALDH3A2 directly. However, certain therapeutic strategies are being explored to alleviate the symptoms of Sjögren-Larsson syndrome (SLS), which is caused by mutations in the ALDH3A2 gene. These include symptomatic management of ichthyosis with moisturizers and emollients to improve the skin condition, physical therapy for spasticity management, and potentially gene therapy approaches to correct the underlying genetic defect in affected individuals. The development of targeted treatments for ALDH3A2-related conditions is an area of active research.
Yes, ALDH3A2 is expressed in various tissues besides the skin, albeit at lower levels. It is found in the liver, brain, adipose tissue, and other organs. It is believed that ALDH3A2's enzyme activity in these tissues is involved in the metabolism of fatty aldehydes and in protecting cells against oxidative damage.
Gene therapy holds promise as a potential treatment for Sjögren-Larsson syndrome (SLS), which is caused by mutations in the ALDH3A2 gene. Preclinical studies using animal models have shown positive results, with gene replacement strategies effectively restoring ALDH3A2 activity and improving symptoms. However, the development of safe and effective gene therapy approaches for SLS is still in the early stages, and more research is needed before it can be considered a viable treatment option for SLS.
ALDH3A2 has not been widely established as a biomarker for specific diseases or conditions. However, ALDH enzymes, including ALDH3A2, have been implicated in certain cancers, such as breast cancer and hepatocellular carcinoma, where their dysregulation may contribute to tumor progression and drug resistance. Further studies are needed to evaluate the potential use of ALDH3A2 as a biomarker for these diseases or other conditions.
Besides its role in lipid metabolism and detoxification, ALDH3A2 has been implicated in other biological processes. Some studies have suggested a potential involvement of ALDH3A2 in cell proliferation, differentiation, and apoptosis. However, the exact mechanisms and significance of these observations are still under investigation. Further research is needed to fully understand the broader biological functions of ALDH3A2.
The regulation of ALDH3A2 protein expression and activity is not yet fully understood. However, studies have indicated that certain transcription factors, such as PPARα (peroxisome proliferator-activated receptor alpha) and AP-1 (activator protein 1), can influence ALDH3A2 gene expression. Additionally, oxidative stress and inflammatory signals have been shown to affect ALDH3A2 activity. Further research is needed to fully elucidate the regulatory mechanisms of ALDH3A2.
ALDH3A2 has been found to interact with various proteins to form functional complexes. For instance, it has been shown to interact with several aldehyde dehydrogenases, such as ALDH1A1 and ALDH1A3. These interactions suggest potential cooperative roles in aldehyde metabolism. ALDH3A2 has also been observed to interact with proteins involved in lipid metabolism, oxidative stress response, and cellular detoxification pathways. Further research is needed to fully understand the interactome of ALDH3A2 and its significance in cellular processes.
The identification of specific natural inhibitors or activators of ALDH3A2 is still an area of ongoing research. However, certain compounds and substances have been found to modulate the activity or expression of ALDH enzymes in general, including ALDH3A2. For example, disulfiram, a drug mainly used in the treatment of alcoholism, has been shown to inhibit various ALDH isoforms, including ALDH3A1 and ALDH1A1. Additionally, certain dietary factors and environmental chemicals may influence ALDH activity. Further studies are needed to determine any specific natural compounds that directly modulate ALDH3A2 activity.
Currently, there is no cure for Sjögren-Larsson syndrome, and treatment focuses on managing the symptoms. Skin care to alleviate ichthyosis, physical and occupational therapies to address spasticity and motor difficulties, and educational support for intellectual disability are among the treatment approaches. Additionally, medications such as retinoids may be prescribed to improve skin symptoms in some cases. However, ongoing research aims to develop targeted therapies that can address the underlying cause of the disease by restoring ALDH3A2 function or reducing the accumulation of fatty aldehydes.
ALDH3A2 is primarily known as an enzyme. It belongs to the aldehyde dehydrogenase enzyme family, which catalyzes the oxidation of aldehydes to their corresponding acids. ALDH enzymes are widely involved in various metabolic pathways. However, like many enzymes, ALDH3A2 does have certain structural characteristics that are important for its function, including specific amino acid residues that contribute to its active site and enzymatic activity.
ALDH3A2 is essential for the normal metabolism of lipids, specifically fatty aldehydes. It catalyzes the conversion of fatty aldehydes into fatty acids, which are essential components of triglycerides, phospholipids, and other lipid molecules. Dysfunction of ALDH3A2 leads to the accumulation of fatty aldehydes, disrupting lipid metabolism and contributing to the pathogenesis of Sjögren-Larsson syndrome.
While mutations in the ALDH3A2 gene are primarily associated with Sjögren-Larsson syndrome, there have been rare reports of individuals with ALDH3A2 mutations exhibiting symptoms that do not fit the classic SLS triad. These atypical presentations include cases with intellectual disability and spasticity but without ichthyosis. However, the exact implications of these variants and their association with other conditions are still being investigated.
Mutations in the ALDH3A2 gene are associated with a rare autosomal recessive disorder called Sjögren-Larsson syndrome (SLS). SLS is characterized by a triad of symptoms including ichthyosis (a scaly skin condition), intellectual disability, and spasticity (stiff, rigid muscles). These mutations result in a deficiency of ALDH3A2 enzyme activity and the subsequent accumulation of fatty aldehydes, leading to the development of SLS.
Customer Reviews (4)
Write a reviewThe bands of proteins in Western Blotting experiments were very clear.
Their expertise and guidance have helped overcome hurdles, ensuring the smooth progress of my research.
Its versatility allows me to explore its diverse roles in various biochemical and biological processes accurately.
Its purity and consistency have provided me with reliable and reproducible results, ensuring the accuracy of my research findings.
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