Dihydrolipoyl Dehydrogenase, Mitochondrial (DLD) Antibody
260€ (50 µg)
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935106861
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name
Dihydrolipoyl Dehydrogenase, Mitochondrial (DLD) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx377509
tested applications
ELISA, WB, IHC
Description
Dihydrolipoyl Dehydrogenase, Mitochondrial (DLD) Antibody is a Rabbit polyclonal antibody for the detection of Human Dihydrolipoyl Dehydrogenase, Mitochondrial (DLD).
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Dihydrolipoyl Dehydrogenase, Mitochondrial (DLD) |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Size 1 | 50 µg |
| Size 2 | 100 µg |
| Form | Liquid |
| Tested Applications | ELISA, WB, IHC |
| Buffer | 0.01 M PBS, pH 7.4, 50% glycerol, 0.05% Proclin-300. |
| Availability | Shipped within 5-12 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | P09622 |
| Gene ID | 1738 |
| NCBI Accession | NP_000099.2 |
| Background | Antibody anti-DLD |
| Status | RUO |
Descripción
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DLD antibody
This gene encodes a member of the class-I pyridine nucleotide-disulfide oxidoreductase family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In homodimeric form, the encoded protein functions as a dehydrogenase and is found in several multi-enzyme complexes that regulate energy metabolism. However, as a monomer, this protein can function as a protease. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency. Alternative splicing results in multiple transcript variants.
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