SLC25A20
Reactivity: Mouse
WB, ELISA, IF (cc), IF (p), IHC (fro), IHC (p)
Host: Rabbit
Polyclonal
unconjugated
Application Notes
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.
Restrictions
For Research Use only
Format
Lyophilized
Reconstitution
Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
Concentration
1 mg/mL
Buffer
Antibody is lyophilized in PBS buffer with 2 % sucrose.
Handling Advice
As with any antibody avoid repeat freeze-thaw cycles.
Storage
4 °C/-20 °C
Storage Comment
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 antibody, BG:DS02740.15 antibody, CACT antibody, CG5848 antibody, Cact antibody, Dmel\\CG5848 antibody, cac antibody, dip6 antibody, fs(2)ltoRN48 antibody, n(2)k17003 antibody, cact antibody, dif-1 antibody, SLC25A20 antibody, DKFZp468F1219 antibody, zgc:77760 antibody, PRKAR2A antibody, CAC antibody, 1110007P09Rik antibody, C78826 antibody, mCAC antibody, cactus antibody, solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 antibody, solute carrier family 25 member 20 antibody, solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 L homeolog antibody, solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 antibody, cact antibody, slc25a20 antibody, SLC25A20 antibody, Slc25a20 antibody, slc25a20.L antibody
Background
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.