Malic Enzyme 2, NADP+ Dependent, Mitochondrial (ME2) Antibody

351€ (100 µg)
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935106861
info@markelab.com
name
Malic Enzyme 2, NADP+ Dependent, Mitochondrial (ME2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx375122
tested applications
ELISA, WB, IHC
Description
Malic Enzyme 2, NADP+ Dependent, Mitochondrial (ME2) Antibody is a Rabbit Polyclonal antibody against Malic Enzyme 2, NADP+ Dependent, Mitochondrial (ME2).
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Primary Antibodies |
Immunogen Target | Malic Enzyme 2, NADP+ Dependent, Mitochondrial (ME2) |
Host | Rabbit |
Reactivity | Human |
Recommended Dilution | Validated in IHC-P. Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | Unconjugated |
Purification | Purified by affinity chromatography using epitope-specific immunogen. |
Size 1 | 100 µg |
Form | Liquid |
Tested Applications | ELISA, WB, IHC |
Buffer | PBS, 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
Availability | Shipped within 5-12 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | P23368 |
Gene ID | 4200 |
Background | Antibody anti-ME2 |
Status | RUO |
Note | Concentration: 1 mg/ml - |
Descripción
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This gene encodes a mitochondrial NAD-dependent malic enzyme, a homotetrameric protein, that catalyzes the oxidative decarboxylation of malate to pyruvate. It had previously been weakly linked to a syndrome known as Friedreich ataxia that has since been shown to be the result of mutation in a completely different gene. Certain single-nucleotide polymorphism haplotypes of this gene have been shown to increase the risk for idiopathic generalized epilepsy. Alternatively spliced transcript variants encoding different isoforms found for this gene. [provided by RefSeq].
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