PMM2 Antikörper (C-Term)

Produktnummer ABIN1536830

Produktdetails anti-PMM2 Antikörper

Target: PMM2 (Phosphomannomutase 2 (PMM2))

Bindungsspezifität: AA 198-226, C-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PMM2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Homologie: B, Pr, M

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

Immunogen: This PMM2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 198-226 amino acids from the C-terminal region of human PMM2.

Klon: RB39495

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

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: PMM2 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Haltbarkeit: 6 months

Details zu PMM2

Target: PMM2 (Phosphomannomutase 2 (PMM2))

Andere Bezeichnung: PMM2 (PMM2 Produkte)

Synonyme: cb626 antikoerper, zgc:56149 antikoerper, MGC82869 antikoerper, pmm2 antikoerper, CDG1 antikoerper, CDG1a antikoerper, CDGS antikoerper, PMI antikoerper, PMI1 antikoerper, PMM 2 antikoerper, AI585868 antikoerper, C86848 antikoerper, phosphomannomutase 2 antikoerper, phosphomannomutase 2 S homeolog antikoerper, pmm2 antikoerper, PMM2 antikoerper, pmm2.S antikoerper, PTRG_02815 antikoerper, Tsp_00480 antikoerper, Pmm2 antikoerper

Hintergrund: The protein encoded by this gene catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate, which is a precursor to GDP-mannose necessary for the synthesis of dolichol-P-oligosaccharides. Mutations in this gene have been shown to cause defects in glycoprotein biosynthesis, which manifests as carbohydrate-deficient glycoprotein syndrome type I. [provided by RefSeq].

Molekulargewicht: 28082

Gen-ID: 5373

NCBI Accession: NP_000294

UniProt: O15305