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Anti-ASL / Argininosuccinate Lyase Antibody (aa101-150) LS-C80446
Most Popular ASL / Argininosuccinate Lyase Antibodies
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Details
| Human ASL / Argininosuccinate Lyase | |
| Rabbit | |
| Human, Monkey, Mouse, Rat, Bat, Bovine, Guinea pig, Hamster, Horse, Pig, Rabbit, Chicken, Xenopus, Zebrafish (tested or 100% immunogen sequence identity) | |
| IgG Polyclonal | |
| Unconjugated. Also available conjugated with Biotin, FITC, HRP. | |
| Immunoaffinity purified | |
| Unmodified |
Applications
- Western blot
- (applications tested for the base form of this product only)
Specificity and Use
| ASL / Argininosuccinate Lyase antibody was raised against synthetic peptide located between aa101-150 of human ASL (P04424, NP_000039). Percent identity by BLAST analysis: Human, Gorilla, Gibbon, Monkey, Marmoset, Mouse, Rat, Hamster, Elephant, Bovine, Bat, Rabbit, Horse, Pig, Opossum, Guinea pig, Zebra finch, Chicken, Platypus, Xenopus, Frog, Smelt, Stickleback, Zebrafish, Sea squirt (100%); Bloom alga (92%). | ||
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| aa101-150 | ||
| Human ASL | ||
| ELISA titer using peptide based assay: 1:62500. Western Blot: Suggested dilution at 0.25 ug/ml in 5% skim milk / PBS buffer, and HRP conjugated anti-Rabbit IgG should be diluted in 1:50000 - 100000 as second antibody. |
Packaging
| Lyophilized from PBS with 2% sucrose | |
| 50 µl Distilled Water. | |
| Long term: -20°C, the use of 50% glycerol is recommended if storing aliquots in -20°C for long term use (up to 1 year); Short term (less than one week): +4°C. Avoid repeat freeze-thaw cycles. | |
| For research use only. |
About ASL / Argininosuccinate Lyase
P04424
NM_000048
NP_000039.2
ASL Antibody, ASAL Antibody, Argininosuccinate lyase Antibody, Argininosuccinase Antibody, Arginosuccinase Antibody
ASL / Argininosuccinate Lyase encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.
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Requested From:
Date Requested: 6/25/2017
Date Requested: 6/25/2017
