This antibody is purified through a protein A column, followed by peptide affinity purification.
Immunogen
This SLC25A20 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 235-264 amino acids from the C-terminal region of human SLC25A20.
SLC25A20
Reactivity: Mouse
WB, ELISA, IF (p), IF (cc), IHC (fro), IHC (p)
Host: Rabbit
Polyclonal
unconjugated
Application Notes
For WB starting dilution is: 1:1000
Restrictions
For Research Use only
Format
Liquid
Concentration
0.5 mg/mL
Buffer
Supplied in PBS with 0.09 % (W/V) sodium azide.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
4 °C,-20 °C
Storage Comment
Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
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
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.