SLC25A20 antibody can be used for detection of SLC25A20 by ELISA at 1:312500. SLC25A20 antibody can be used for detection of SLC25A20 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Beschränkungen
Nur für Forschungszwecke einsetzbar
Format
Lyophilized
Rekonstitution
Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
Konzentration
1 mg/mL
Buffer
Antibody is lyophilized in PBS buffer with 2 % sucrose.
Handhabung
As with any antibody avoid repeat freeze-thaw cycles.
Lagerung
4 °C/-20 °C
Informationen zur Lagerung
For short periods of storage (days) store at 4 °C. For longer periods of storage, store SLC25A20 antibody at -20 °C.
Target
SLC25A20
(Solute Carrier Family 25 (Carnitine/acylcarnitine Translocase), Member 20 (SLC25A20))
5848 antikoerper, BG:DS02740.15 antikoerper, CACT antikoerper, CG5848 antikoerper, Cact antikoerper, Dmel\\CG5848 antikoerper, cac antikoerper, dip6 antikoerper, fs(2)ltoRN48 antikoerper, n(2)k17003 antikoerper, cact antikoerper, dif-1 antikoerper, SLC25A20 antikoerper, DKFZp468F1219 antikoerper, zgc:77760 antikoerper, PRKAR2A antikoerper, CAC antikoerper, 1110007P09Rik antikoerper, C78826 antikoerper, mCAC antikoerper, cactus antikoerper, solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 antikoerper, solute carrier family 25 member 20 antikoerper, solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 L homeolog antikoerper, solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 antikoerper, cact antikoerper, slc25a20 antikoerper, SLC25A20 antikoerper, Slc25a20 antikoerper, slc25a20.L antikoerper
Hintergrund
SLC25A20 is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space.It mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants.This gene product is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. This protein mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.