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Western blot analysis of lysates from HepG2 cell line and mouse kidney, rat spleen tissue lysates(from left to right), using ACADL Antibody at 1:1000 at each lane.
Western blot analysis of lysates from HepG2 cell line and mouse kidney, rat spleen tissue lysates(from left to right), using ACADL Antibody at 1:1000 at each lane.

ACADL Antibody

CATALOG NUMBER: 56-871

Clonality:
Polyclonal
Tested Applications:
WB
Host Species:
Rabbit
Species Reactivity:
Human, Mouse, Rat
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human, Mouse, Rat
Immunogen:
This ACADL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 14-43 amino acids from the N-terminal region of human ACADL.
Conjugate:
Unconjugated
Tested Applications:
WB
Application Note:
For WB starting dilution is: 1:1000
Predicted Molecular Weight:
48 kDa
Purification:
This antibody is purified through a protein A column, followed by peptide affinity purification.
Clonality:
Polyclonal
Isotype:
Rabbit Ig
physical-state:
Liquid
Buffer:
Supplied in PBS with 0.09% (W/V) sodium azide.
Concentration:
batch dependent
Storage Conditions:
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.
Ncbi Official Symbol:
ACADL
Additional Names:
Long-chain specific acyl-CoA dehydrogenase, mitochondrial, LCAD, ACADL
Protein Accession Number:
P28330
Protein Gi Number:
223590148
Ncbi Gene Id Number:
33
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
The protein encoded by this gene belongs to the acyl-CoAdehydrogenase family, which is a family of mitochondrialflavoenzymes involved in fatty acid and branched chain amino-acidmetabolism. This protein is one of the four enzymes that catalyzethe initial step of mitochondrial beta-oxidation of straight-chainfatty acid. Defects in this gene are the cause of long-chainacyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotichypoglycemia.
Background Reference 1:
Bailey, S.D., et al. Diabetes Care 33(10):2250-2253(2010)
Background Reference 2:
Maher, A.C., et al. Mol. Genet. Metab. 100(2):163-167(2010)
Background Reference 3:
Illig, T., et al. Nat. Genet. 42(2):137-141(2010)
Background Reference 4:
Talmud, P.J., et al. Am. J. Hum. Genet. 85(5):628-642(2009)

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.

CATALOG NUMBER:

56-871

List Size:
400 ul

List Price:

$495.00

Datasheet
Shipping Info

$65 Standard Overnight flat rate for as many products shipped within the United States.

$35 Dry Ice Shipment fee may be required on some items.

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