| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| XRCC5-ACADL-20-RERE | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-REOR | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-REGO | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-REGR | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-REAQ | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-ORRE | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-OROR | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-ORGO | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-ORGR | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-ORAQ | 20 (40 μL) | 200 μL |
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| XRCC5-ACADL-20-GORE | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-GOOR | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-GOGO | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-GOGR | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-GOAQ | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-GRRE | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-GROR | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-GRGO | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-GRGR | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-GRAQ | 20 (40 μL) | 200 μL |
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| XRCC5-ACADL-20-AQRE | 20 (40 μL) | 200 μL |
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| XRCC5-ACADL-20-AQOR | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-AQGO | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-AQGR | 20 (40 μL) | 200 μL |
|
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| XRCC5-ACADL-20-AQAQ | 20 (40 μL) | 200 μL |
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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. [provided by RefSeq, Jul 2008]
Gene Symbol : ACADL
Gene Name : Acyl-CoA dehydrogenase long chain
Chromosome : CHR 2: 210,225,490-210,187,989
Locus : 2q34
The protein encoded by this gene is the 80-kilodalton subunit of the Ku heterodimer protein which is also known as ATP-dependant DNA helicase II or DNA repair protein XRCC5. Ku is the DNA-binding component of the DNA-dependent protein kinase, and it functions together with the DNA ligase IV-XRCC4 complex in the repair of DNA double-strand break by non-homologous end joining and the completion of V(D)J recombination events. This gene functionally complements Chinese hamster xrs-6, a mutant defective in DNA double-strand break repair and in ability to undergo V(D)J recombination. A rare microsatellite polymorphism in this gene is associated with cancer in patients of varying radiosensitivity. [provided by RefSeq, Jul 2008]
Gene Symbol : XRCC5
Gene Name : X-ray repair cross complementing 5
Chromosome : CHR 2: 216,109,296-216,206,292
Locus : 2q35
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