Recombinant Mouse PDHA1 Protein
Cat.No. : | PDHA1-12572M |
Product Overview : | Recombinant Mouse PDHA1 full length or partial length protein was expressed. |
- Specification
- Gene Information
- Related Products
Source : | Mammalian Cells |
Species : | Mouse |
Tag : | His |
Form : | Liquid or lyophilized powder |
Endotoxin : | < 1.0 EU per μg of the protein as determined by the LAL method. |
Purity : | >80% |
Notes : | This item requires custom production and lead time is between 5-9 weeks. We can custom produce according to your specifications. |
Storage : | Store it at +4 ºC for short term. For long term storage, store it at -20 ºC~-80 ºC. |
Storage Buffer : | PBS buffer |
Gene Name : | Pdha1 pyruvate dehydrogenase E1 alpha 1 [ Mus musculus ] |
Official Symbol : | PDHA1 |
Gene ID : | 18597 |
mRNA Refseq : | NM_008810.2 |
Protein Refseq : | NP_032836.1 |
MIM : | |
UniProt ID : | P35486 |
Products Types
◆ Recombinant Protein | ||
PDHA1-6598M | Recombinant Mouse PDHA1 Protein, His (Fc)-Avi-tagged | +Inquiry |
Pdha1-4760M | Recombinant Mouse Pdha1 Protein, Myc/DDK-tagged | +Inquiry |
PDHA1-3173R | Recombinant Rhesus Macaque PDHA1 Protein, His (Fc)-Avi-tagged | +Inquiry |
PDHA1-825H | Recombinant Human PDHA1 Protein, MYC/DDK-tagged | +Inquiry |
PDHA1-1635H | Recombinant Human PDHA1 Protein, His (Fc)-Avi-tagged | +Inquiry |
◆ Lysates | ||
PDHA1-001HCL | Recombinant Human PDHA1 cell lysate | +Inquiry |
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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