NAD-ME Antikörper (C-Term)

Produktnummer ABIN656541

Produktdetails anti-NAD-ME Antikörper

Target: NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))

Bindungsspezifität: AA 527-556, C-Term

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NAD-ME Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This ME2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 527-556 amino acids from the C-terminal region of human ME2.

Klon: RB32070

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000. IHC-P: 1:10~50

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: ME2 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Haltbarkeit: 6 months

Details zu NAD-ME

Target: NAD-ME (NAD Dependent Malate Dehydrogenase (NAD-ME))

Andere Bezeichnung: ME2 (NAD-ME Produkte)

Synonyme: ODS1 antikoerper, AW120568 antikoerper, D030040L20Rik antikoerper, NAD-ME antikoerper, zgc:100941 antikoerper, malic enzyme 2 antikoerper, malic enzyme 2, NAD(+)-dependent, mitochondrial antikoerper, malic enzyme 2, NAD(+)-dependent, mitochondrial S homeolog antikoerper, ME2 antikoerper, Me2 antikoerper, me2.S antikoerper, me2 antikoerper

Hintergrund: 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].

Molekulargewicht: 65444

Gen-ID: 4200

NCBI Accession: NP_001161807, NP_002387

UniProt: P23368

Pathways: Production of Molecular Mediator of Immune Response