ACADL polyclonal antibody

Catalog # PAB18529

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Size:100 ug
Price: USD $ 346.00
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  • +1-909-264-1399
    +1-909-992-0619
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  • +1-909-992-3401
Images
Western Blot (Tissue lysate)
Application

Western Blot (Tissue lysate)

Western blot analysis of human fetal kidney lysate with ACADL polyclonal antibody (Cat # PAB18529) at 1 : 500 dilution.

  • Specifications

    Product Description

    Rabbit polyclonal antibody raised against partial recombinant ACADL.

    Immunogen

    Recombinant protein corresponding to amino acids 198-408 of human ACADL.

    Host

    Rabbit

    Reactivity

    Human

    Specificity

    This antibody is specific to ACADL.

    Form

    Liquid

    Purification

    Protein A purification

    Recommend Usage

    Western Blot (1:500-1:1000)
    ELISA (1:20000-1:80000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In buffer containing 0.02% sodium azide

    Storage Instruction

    Store at 4°C for three months. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

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

  • Applications

    Western Blot (Tissue lysate)

    Western blot analysis of human fetal kidney lysate with ACADL polyclonal antibody (Cat # PAB18529) at 1 : 500 dilution.

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — ACADL

    Entrez GeneID

    33

    GeneBank Accession#

    BC039063

    Gene Name

    ACADL

    Gene Alias

    ACAD4, FLJ94052, LCAD

    Gene Description

    acyl-Coenzyme A dehydrogenase, long chain

    Omim ID

    201460 609576

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq

    Other Designations

    long-chain specific acyl-CoA dehydrogenase

  • Interactomes
  • Pathways
  • Diseases
  • Publication Reference
    • Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.

      Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD, Collins FS, Wagner L, Shenmen CM, Schuler GD, Altschul SF, Zeeberg B, Buetow KH, Schaefer CF, Bhat NK, Hopkins RF, Jordan H, Moore T, Max SI, Wang J, Hsieh F, Diatchenko L, Marusina K, Farmer AA, Rubin GM, Hong L, Stapleton M, Soares MB, Bonaldo MF, Casavant TL, Scheetz TE, Brownstein MJ, Usdin TB, Toshiyuki S, Carninci P, Prange C, Raha SS, Loquellano NA, Peters GJ, Abramson RD, Mullahy SJ, Bosak SA, McEwan PJ, McKernan KJ, Malek JA,

      PNAS 2002 Dec; 99(26):16899.

Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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