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Rabbit anti-Human ASL Polyclonal Antibody

The antibody against ASL was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 289-464 of human ASL (NP_000039.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, IF/ICC, ELISA.

ADA-09500A

The antibody against ASL was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 289-464 of human ASL (NP_000039.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, IF/ICC, ELISA.

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Specifications


Cat.No ADA-09500A ClonalityPolyclonal
Host SpeciesRabbitTarget NameASL
Target SynonymsASAL; ASLFormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.01% thimerosal, pH7.3.Purification MethodAffinity purification
Positive SamplesHeLa, Mouse kidney, HepG2, Mouse brain, Mouse liver, Rat liver, SH-SY5YApplicationELISA, WB, IF/ICC, IHC-P

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 289-464 of human ASL (NP_000039.2).Target SpeciesHuman
Immunogen SequenceNPDSLELIRSKAGRVFGRCAGLLMTLKGLPSTYNKDLQEDKEAVFEVSDTMSAVLQVATGVISTLQIHQENMGQALSPDMLATDLAYYLVRKGMPFRQAHEASGKAVFMAETKGVALNQLSLQELQTISPLFSGDVICVWDYGHSVEQYGALGGTARSSVDWQIRQVRALLQAQQAUniprot IDP04424
Background Information
  • Uniprot Id

    P04424

  • Target Species

    Human

  • Target Name

    ASL

  • Target Full Name

    Argininosuccinate lyase

  • Target Involvement

    Argininosuccinic aciduria (ARGINSA)

  • Target Protein Families

    Lyase 1 family, Argininosuccinate lyase subfamily

  • Target Synonyms

    Argininosuccinase; Argininosuccinate lyase; Arginosuccinase; ARLY_HUMAN; ASAL; ASL; EC 4.3.2.1

  • Target Background

    This gene 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. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described.

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