PEX12 Antikörper (Middle Region)

Produktnummer ABIN5515310

Produktdetails anti-PEX12 Antikörper

Target: PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))

Bindungsspezifität: Middle Region

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PEX12 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: SIMFLVLLPY LKVKLEKLVS SLREEDEYSI HPPSSRWKRF YRAFLAAYPF

Aufreinigung: Affinity purified

Immunogen: The immunogen is a synthetic peptide directed towards the middle region of human PEX12

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Details zu PEX12

Target: PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))

Andere Bezeichnung: PEX12 (PEX12 Produkte)

Synonyme: zgc:56182 antikoerper, pex12 antikoerper, MGC81372 antikoerper, PEX12 antikoerper, DDBDRAFT_0186545 antikoerper, DDBDRAFT_0238076 antikoerper, DDB_0186545 antikoerper, DDB_0238076 antikoerper, LOC100226224 antikoerper, PAF-3 antikoerper, PBD3A antikoerper, Peroxin-12 antikoerper, AI451906 antikoerper, peroxisomal biogenesis factor 12 antikoerper, peroxisomal biogenesis factor 12 L homeolog antikoerper, RING zinc finger-containing protein antikoerper, pex12 antikoerper, PEX12 antikoerper, pex12.L antikoerper, Pex12 antikoerper

Hintergrund: This gene belongs to the peroxin-12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS).

Alias Symbols: PAF-3, PBD3A

Protein Size: 167

Gen-ID: 5193

NCBI Accession: NM_000286, NP_000277

UniProt: O00623