SLC27A2 monoclonal antibody, clone 6B3A9
* The price is valid only in USA. Please select country.
-
More Files
- More Functions
-
Specification
Product Description
Mouse monoclonal antibody raised against recombinant human SLC27A2.
Immunogen
Recombinant protein corresponding to amino acids 346-405 of human SLC27A2 from E. coli.
Host
Mouse
Theoretical MW (kDa)
70.3
Reactivity
Human
Form
Liquid
Isotype
IgG1
Recommend Usage
ELISA (1:10000)
Flow Cytometry
Immunocytochemistry
Immunohistochemistry (1:200-1:1000)
Western Blot (1:500-1:2000)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.05% sodium azide).
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
Applications
Western Blot (Transfected lysate)
Western blot analysis of (1) HEK293 cells, (2) SLC27A2-hIgGFc transfected HEK293 cell lysate with SLC27A2 monoclonal antibody.Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of paraffin-embedded liver cancer tissue with SLC27A2 monoclonal antibody.Enzyme-linked Immunoabsorbent Assay
ELISA analysis of SLC27A2 monoclonal antibody, clone 6B3A9. -
Gene Info — SLC27A2
Entrez GeneID
11001Gene Name
SLC27A2
Gene Alias
ACSVL1, FACVL1, FATP2, HsT17226, VLACS, VLCS, hFACVL1
Gene Description
solute carrier family 27 (fatty acid transporter), member 2
Omim ID
603247Gene Ontology
HyperlinkGene Summary
The protein encoded by this gene is an isozyme of long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme activates long-chain, branched-chain and very-long-chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney, and is present in both endoplasmic reticulum and peroxisomes, but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
Other Designations
very long-chain fatty-acid-coenzyme A ligase 1|very-long-chain acyl-CoA synthetase
-
Interactome
-
Pathway
-
Disease
- +1-909-264-1399
+1-909-992-0619
Toll Free : +1-877-853-6098 - +1-909-992-3401
- sales@abnova.com