PEX10 Antikörper (Middle Region)

Produktnummer ABIN2781270

Produktdetails anti-PEX10 Antikörper

Target: PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

Bindungsspezifität: Middle Region

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PEX10 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC)

Sequenz: QALRPDPLRV LMSVAPSALQ LRVRSLPGED LRARVSYRLL GVISLLHLVL

Homologie: Human: 100%

Produktmerkmale: This is a rabbit polyclonal antibody against PEX10. It was validated on Western Blot and immunohistochemistry.

Aufreinigung: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the middle region of human PEX10

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator.

Kommentare:

Antigen size: 346 AA

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: Lot specific

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.

Handhabung: Avoid repeated freeze-thaw cycles.

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 PEX10

Target: PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

Andere Bezeichnung: PEX10 (PEX10 Produkte)

Hintergrund: PEX10 is a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in PEX10 gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome.This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms.
Alias Symbols: MGC1998, NALD, RNF69
Protein Interaction Partner: HNRNPD, PEX5, PEX14, LIG4, PCGF6, CGRRF1, MKRN3, PEX19, PEX12, PEX10, UBC, UBE2I, PEX2,
Protein Size: 346

Molekulargewicht: 39 kDa

Gen-ID: 5192

NCBI Accession: NM_153818, NP_722540

Pathways: Monocarboxylic Acid Catabolic Process