Human ASS1 antibody
ASS1 (argininosuccinate synthase or citrulline-aspartate ligase) belongs to the argininosuccinate synthase family. ASS1 is a urea cycle enzyme that is essential in the conversion of nitrogen from ammonia and aspartate to urea. A deficiency of ASS1 causes citrullinemia (CTLN1), an autosomal recessive disease which is characterized by severe vomiting spells and mental retardation. Cells deficient in ASS1 must absorb the arginine they need for growth from circulating blood.
Product Specifications
Product Name Alternative
Argininosuccinate synthase, ASS, CTLN1, Argininosuccinate synthase
Host
Mouse
Antigen Species
Human
Reactivity
Human
Immunogen
Recombinant human ASS1 (1-412aa) purified from E. coli
Clonality
Monoclonal
Isotype
IgG2a κ
Clone
AT1G11
Conjugation
Unconjugated
Applications
ELISA, WB, ICC/IF
Purification Method
By protein-A affinity chromatography
Concentration
1 mg/mL (determined by BCA assay)
Additionnal Information
References & Citations
Storage Conditions
Can be stored at 2°C to 8°C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
Formulation
Liquid in. Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% glycerol
Applications Notes
Scientific Category
Signal Transduction
NCBI Accession Number
NP_000041
Uniprot Accession Number
P00966
WB Description
IF Description
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