Analytical Data
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Gene name
ACAD8
- Application
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Alternative Names
ACAD8；ARC42；IBD；Isobutyryl-CoA dehydrogenase. mitochondrial
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Species
Human
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Source
E. coli
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Tag
His tag N-Terminus
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Purity
Greater than 90% as determined by SDS-PAGE.
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Uniprot
Q9UKU7
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Expression Region
23-415aa
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AA Sequence
MGSSHHHHHH SSGLVPRGSH MGSLVQTGHR SLTSCIDPSM GLNEEQKEFQ KVAFDFAARE MAPNMAEWDQ KELFPVDVMR KAAQLGFGGV YIQTDVGGSG LSRLDTSVIF EALATGCTST TAYISIHNMC AWMIDSFGNE EQRHKFCPPL CTMEKFASYC LTEPGSGSDA ASLLTSAKKQ GDHYILNGSK AFISGAGESD IYVVMCRTGG PGPKGISCIV VEKGTPGLSF GKKEKKVGWN SQPTRAVIFE DCAVPVANRI GSEGQGFLIA VRGLNGGRIN IASCSLGAAH ASVILTRDHL NVRKQFGEPL ASNQYLQFTL ADMATRLVAA RLMVRNAAVA LQEERKDAVA LCSMAKLFAT DECFAICNQA LQMHGGYGYL KDYAVQQYVR DSRVHQILEG SNEVMRILIS RSLLQE
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Molecular Weight
45 kDa
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Endotoxin
< 1.0 EU per μg protein as determined by the LAL method.
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Form
Freeze-dried powder
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Buffer formulation
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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Reconstitution
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- Customization
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Stability Test
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
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Storage & Shelf Life
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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Shipping
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
Related Products
Protein Description
ACAD8, or Acyl-CoA Dehydrogenase Family Member 8, is an essential enzyme in the mitochondrial fatty acid beta-oxidation pathway, specifically involved in the metabolism of medium-chain fatty acids. Its primary role is to catalyze the dehydrogenation of acyl-CoA substrates, which is crucial for the energy production in cells. Deficiencies or mutations in the ACAD8 gene have been linked to metabolic disorders, highlighting the enzyme's importance in maintaining lipid homeostasis and cellular energy balance. Recent research into recombinant ACAD8 proteins has gained traction, aiming to better understand its structure-function relationship and the mechanisms underlying its enzymatic activity. This investigation not only sheds light on the biochemical pathways involved in fatty acid metabolism but also has potential therapeutic implications for treating metabolic diseases. By characterizing ACAD8 through recombinant technology, scientists can explore its role in various metabolic conditions, paving the way for innovative treatment strategies and a deeper understanding of mitochondrial dysfunction.
