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ACADL Antibody (N-term)Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)
| Country | United States
Ordering Information
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| Catalog # | Size | Availability | Price | |
| AP13134a | 0.1 mg 400 ul | In Stock | $ 255.00 | DISCONTINED INQUIRE CLICK INQUIRE Add to cart |
| AP13134a-ev20 | 20 ug 100 ul | In Stock | $ 95.00 | DISCONTINED INQUIRE CLICK INQUIRE Add to cart |
- Specification
- Citiations : 0
- Reviews
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- Backgrounds
ACADL Antibody (N-term) - Product info | |
| Application | WB
|
| Primary Accession | P28330 |
| Other Accession | NP_001599.1 |
| Reactivity | Mouse |
| Concentration | 0.25 mg/ml |
| Isotype | Rabbit Ig |
| Calculated MW | 47656 Da |
ACADL Antibody (N-term) - Additional info | |
| Gene ID 33 | |
| Other Names ACADL; Long-chain specific acyl-CoA dehydrogenase, mitochondrial | |
| Target/Specificity This ACADL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 13-43 amino acids from the N-terminal region of human ACADL. | |
| Dilution WB~~1:100~500WB~~1:1000 | |
| Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. | |
| Storage Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. | |
| Precautions ACADL Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures. | |
ACADL Antibody (N-term) - Protein Information | |
| Name ACADL | |
| Cellular Location Mitochondrion matrix. | |
ACADL Antibody (N-term) - Related products
AP13134a: ACADL Antibody (N-term)
AP8536c: ACADL Antibody (Center)
RI10040: ACADL predesign siRNA
DC07238: Human ACADL cDNA Clone
ACADL Antibody (N-term) - Application data
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ACADL Antibody (N-term) (Cat. #AP13134a) western blot analysis in mouse kidney tissue lysates (35ug/lane).This demonstrates the ACADL antibody detected the ACADL protein (arrow).
ACADL Antibody (N-term) - Research Areas
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BACKGROUND
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.
REFERENCES
Bailey, S.D., et al. Diabetes Care 33(10):2250-2253(2010) Maher, A.C., et al. Mol. Genet. Metab. 100(2):163-167(2010) Illig, T., et al. Nat. Genet. 42(2):137-141(2010) Talmud, P.J., et al. Am. J. Hum. Genet. 85(5):628-642(2009) Lu, Y., et al. J. Lipid Res. 49(12):2582-2589(2008)
