ASS1 Antibody (Clone AT1G11)

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number MA01099
Size 100 µL
Host Type Mouse
Immunogen Recombinant human ASS1 (1-412aa) purified from E. coli
Specificity
Isotype Mouse IgG2a, k
Reacitivity Human
Clone Anti-human ASS1 mAb, clone AT1G11, is derived from hybridization of mouse F0 myeloma cells with spleen cells from BALB/c mice immunized with a recombinant human ASS1 protein.
Uniprot
Concentration 1mg/ml
Dilution
Formulation Liquid. In Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% Glycerol.
Application ELISA, WB, Flow cytometry, ICC/IF
Other Names Argininosuccinate synthase, ASS, CTLN1, Argininosuccinate synthase
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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