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ASL antibody (AA 1-300)

This anti-ASL antibody is a Rabbit Polyclonal antibody detecting ASL in WB, IHC and IF. Suitable for Human.
Catalog No. ABIN6137201

Quick Overview for ASL antibody (AA 1-300) (ABIN6137201)

Target

See all ASL Antibodies
ASL (Argininosuccinate Lyase (ASL))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This ASL antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

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    AA 1-300

    Sequence

    MASESGKLWG GRFVGAVDPI MEKFNASIAY DRHLWEVDVQ GSKAYSRGLE KAGLLTKAEM DQILHGLDKV AEEWAQGTFK LNSNDEDIHT ANERRLKELI GATAGKLHTG RSRNDQVVTD LRLWMRQTCS TLSGLLWELI RTMVDRAEAE RDVLFPGYTH LQRAQPIRWS HWILSHAVAL TRDSERLLEV RKRINVLPLG SGAIAGNPLG VDRELLRAEL NFGAITLNSM DATSERDFVA EFLFWASLCM THLSRMAEDL ILYCTKEFSF VQLSDAYSTG SSLMPQKKNP DSLELIRSKA

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-300 of human ASL (NP_000039.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    ASL (Argininosuccinate Lyase (ASL))

    Alternative Name

    ASL

    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.,ASL,ASAL,Cancer,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,ASL

    Molecular Weight

    48 kDa/49 kDa/51 kDa

    Gene ID

    435

    UniProt

    P04424

    Pathways

    Response to Growth Hormone Stimulus
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