Recombinant Human PDHA1 Protein (Phe30-Ser390), N-His tagged
Cat.No. : | PDHA1-4853H |
Product Overview : | Recombinant human PDHA1 (Phe30-Ser390) fused with the N-His tag was expressed in E. coli. |
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Source : | E. coli |
Species : | Human |
Tag : | N-His |
Form : | Lyophilized powder/frozen liquid |
Molecular Mass : | 42.54 kDa |
Protein Length : | Phe30-Ser390 |
Purity : | >90% as determined by SDS-PAGE. |
Notes : | For research use only. |
Storage : | Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8 centigrade for one week. Store at -20 to -80 centigrade for twelve months from the date of receipt. |
Storage Buffer : | 0.01M PBS, pH 7.4, 0.02% NLS |
Reconstitution : | Reconstitute in sterile water for a stock solution. |
Shipping : | They are shipped out with dry ice/blue ice unless customers require otherwise. |
Gene Name : | PDHA1 pyruvate dehydrogenase (lipoamide) alpha 1 [ Homo sapiens (human) ] |
Official Symbol : | PDHA1 |
Synonyms : | PDHA1; pyruvate dehydrogenase (lipoamide) alpha 1; PDHA; pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial; PDHE1-A type I; pyruvate dehydrogenase complex, E1-alpha polypeptide 1; PHE1A; PDHCE1A; |
Gene ID : | 5160 |
mRNA Refseq : | NM_000284 |
Protein Refseq : | NP_000275 |
MIM : | 300502 |
UniProt ID : | P08559 |
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Related Gene
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 (5)
Ask a questionSymptoms may include developmental delay, intellectual disability, muscle weakness, and movement disorders.
Treatment may involve dietary modifications, supplements, and supportive therapies to manage symptoms.
Yes, researchers are studying potential gene therapy approaches and novel treatments for PDHA1-related disorders.
The PDHA1 protein is critical for supplying energy to the brain, and mutations can lead to neurological impairments.
Mutations in the PDHA1 gene can lead to pyruvate dehydrogenase complex deficiency, resulting in neurological and developmental problems.
Customer Reviews (3)
Write a reviewIncorporating the PDHA1 protein into your research will not only meet but exceed your expectations, enabling you to advance your scientific discoveries with confidence.
Researchers can leverage the unique properties of the PDHA1 protein to gain insights into its biological functions and its impact on disease mechanisms.
It has been shown to play a crucial role in multiple cellular processes, making it highly valuable for investigations into cell signaling, inflammation, and immune responses.
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