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          • Primary Antibodies ›
          • ADSL Antibodies

          Bioss

          Adenylosuccinate Lyase Polyclonal Antibody

          View all (17) ADSL antibodies
          Datasheet
          Protocols
          Questions & Answers
          Datasheet
          Protocols
          Questions & Answers

          Cite Adenylosuccinate Lyase Polyclonal Antibody

          Product Details

          BS-6352R

          Applications
          Tested Dilution
          Publications

          Immunohistochemistry (Paraffin) (IHC (P))

          Assay-dependent
          -

          Immunohistochemistry (Frozen) (IHC (F))

          1:100-1:500
          -

          Immunocytochemistry (ICC/IF)

          1:50-1:200
          -

          ELISA (ELISA)

          1:500-1:1,000
          -
          Product Specifications

          Species Reactivity

          Human, Mouse, Rat

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          KLH conjugated synthetic peptide derived from human Adenylosuccinate Lyase, amino acids 185-280.
          View immunogen

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          1 mg/mL

          Purification

          Protein A

          Storage buffer

          0.01M TBS, pH 7.4, with 50% glycerol, 1% BSA

          Contains

          0.02% ProClin 300

          Storage conditions

          -20°C

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          Target Information

          ADSL (adenylosuccinate lyase), also known as AMPS, ASL or ASASE, is a 484 amino acid protein that is involved in both purine biosynthesis and in the formation of adenosine monophosphate (AMP) from inosine monophosphate. Expressed ubiquitously, ADSL catalyzes two key reactions in AMP biosynthesis, namely the removal of a fumarate from succinylaminoimidazole carboxamide (SAICA) ribotide to give aminoimidazole carboxamide ribotide (AICA) and the subsequent removal of fumarate from adenylosuccinate to yield AMP. Defects in the gene encoding ADSL are the cause of adenylosuccinase deficiency (ADSL deficiency), an autosomal recessive disorder characterized by epilepsy, growth retardation and muscular wasting. Multiple isoforms of ADSL exist due to alternative splicing events.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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          Cite this product

          Bioinformatics

          Protein Aliases: Adenylosuccinase; Adenylosuccinate lyase; adenylosuccinate lyase 1; ADSL; ASase; ASL; test

          View more View less

          Gene Aliases: Adl; ADSL; AMPS; ASASE; ASL; null

          View more View less

          UniProt ID: (Human) P30566, (Mouse) P54822

          View more View less

          Entrez Gene ID: (Human) 158, (Rat) 315150, (Mouse) 11564

          View more View less

          Function(s)
          N6-(1,2-dicarboxyethyl)AMP AMP-lyase (fumarate-forming) activity (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido)succinate AMP-lyase (fumarate-forming) activity catalytic activity lyase activity
          Process(es)
          response to hypoxia purine nucleotide metabolic process AMP biosynthetic process 'de novo' IMP biosynthetic process response to nutrient metabolic process aerobic respiration ribonucleoside monophosphate biosynthetic process response to muscle activity response to starvation 'de novo' AMP biosynthetic process protein tetramerization purine nucleotide biosynthetic process purine ribonucleoside monophosphate biosynthetic process purine ribonucleotide biosynthetic process
          It has to be done as per old AB suggested Products section.
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