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Invitrogen™ Human DCBLD2/ESDN ELISA Kit
Description
Human DCBLD2/ESDN quantitates human DCBLD2/ESDN in serum, plasma, supernatant. The assay will exclusively recognize both natural and recombinant human DCBLD2/ESDN.
This protein is a key enzyme in the catabolic pathway of odd-chain fatty acids, isoleucine, threonine, methionine, and valine. It is probably a dodecamer composed of six biotin-containing alpha subunits and six beta subunits. The protein is located in the mitochondrial matrix. Defects in PCCA are the cause o fpropionic acidemia type I (PA-1) [MIM:606054]. PA-1 is a life-threatening disease characterized by episodic vomiting, lethargy and ketosis, neutropenia, periodic thrombocytopenia, hypogammaglobulinemia, develop-mental retardation, and intolerance to protein.
Spécifications
Spécifications
| Numéro d'enregistrement | 1700055P21Rik; AW146002; CLCP1; coagulation factor V/VIII-homology domains protein 1; CUB, LCCL and coagulation factor V/VIII-homology domains protein 1; Dcbld2; discoidin; discoidin, CUB and LCCL domain containing 2; discoidin, CUB and LCCL domain-containing protein 2; Endothelial and smooth muscle cell-derived neuropilin-like protein; Esdn |
| Plage de l'essai | 0.041 to 10 ng/mL |
| Sensibilité d’essai | 0.041 ng/mL |
| Conjugué | HRP |
| Type de produit | ELISA |
| Type d’échantillon | Plasma, Serum, Supernatant |
| À utiliser avec (équipement) | Colorimetric Microplate Reader |
| ID du gène (Entrez) | 131566 |
| Symbole de gène | DCBLD2 |
| CV intra-essai | <12%, <10 |
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