ACADM Mouse Monoclonal Antibody [Clone ID: OTI2G7]

CAT#: CF811761

Carrier-free (BSA/glycerol-free) ACADM mouse monoclonal antibody,clone OTI2G7

Formulation: Standard Carrier-Free


  View other "OTI2G7" antibodies (4)

USD 600.00

3 Days*

Size
    • 100 ug

Frequently bought together (1)
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    • 200 ug

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Specifications

Product Data
Clone Name OTI2G7
Applications IHC, WB
Recommended Dilution WB 1:2000, IHC 1:500
Reactivities Human, Mouse, Rat
Host Mouse
Isotype IgG1
Clonality Monoclonal
Immunogen Full length human recombinant protein of human ACADM (NP_000007) produced in HEK293T cell.
Formulation Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Reconstitution Method For reconstitution, we recommend adding 100uL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiment, we strongly recommend performing another round of desalting process. (OriGene recommends Zeba Spin Desalting Columns, 7KMWCO from Thermo Scientific)
Purification Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
Conjugation Unconjugated
Storage Store at -20°C as received.
Stability Stable for 12 months from date of receipt.
Predicted Protein Size 46.59 kDa
Gene Name Homo sapiens acyl-CoA dehydrogenase medium chain (ACADM), transcript variant 1, mRNA; nuclear gene for mitochondrial product.
Background This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Synonyms ACAD1; MCAD; MCADH
Reference Data
Protein Families Druggable Genome
Protein Pathways beta-Alanine metabolism, Fatty acid metabolism, Metabolic pathways, PPAR signaling pathway, Propanoate metabolism, Valine, leucine and isoleucine degradation

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*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.