ABCD3
Reaktivität: Human
WB, IF (cc), IF (p)
Wirt: Kaninchen
Polyclonal
AbBy Fluor® 647
Applikationshinweise
The stated application concentrations are suggested starting amounts. Titration of the PMP70 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 0.5-1 μg/mL,IHC (Paraffin): 0.5-1 μg/mL
Beschränkungen
Nur für Forschungszwecke einsetzbar
Buffer
0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
Lagerung
-20 °C
Informationen zur Lagerung
After reconstitution, the PMP70 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
Target
PMP70 (ABCD3)
(ATP-Binding Cassette, Sub-Family D (Ald), Member 3 (ABCD3))
ABC43 antikoerper, PMP70 antikoerper, PXMP1 antikoerper, ZWS2 antikoerper, AI313901 antikoerper, AU018866 antikoerper, AW146054 antikoerper, PMP68 antikoerper, Pxmp1 antikoerper, ABCD3 antikoerper, fb59g09 antikoerper, fd60b04 antikoerper, zgc:55740 antikoerper, wu:fb59g09 antikoerper, wu:fd60b04 antikoerper, pmp70 antikoerper, si:dkey-61d19.3 antikoerper, ATP binding cassette subfamily D member 3 antikoerper, ATP-binding cassette, sub-family D (ALD), member 3 antikoerper, ATP-binding cassette, sub-family D (ALD), member 3a antikoerper, ATP binding cassette subfamily D member 3 S homeolog antikoerper, ATP-binding cassette sub-family D member 3 antikoerper, ATP-binding cassette, sub-family D (ALD), member 3b antikoerper, ABCD3 antikoerper, Abcd3 antikoerper, abcd3a antikoerper, abcd3.S antikoerper, abcd3 antikoerper, LOC100633340 antikoerper, abcd3b antikoerper
Hintergrund
70 kDa peroxisomal membrane protein (PMP70), also called ATP-binding cassette sub-family D member 3, is a protein that in humans is encoded by the ABCD3 gene. The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. The gene was assigned to human chromosome 1p21-p22 by in situ hybridization. This peroxisomal membrane protein likely plays an important role in peroxisome biogenesis. Mutations have been associated with some forms of Zellweger syndrome, a heterogeneous group of peroxisome assembly disorders.