AGA mouse monoclonal antibody (hybridoma)

Catalog # H00000175-M

Size

Price

Stock

Quantity

Size:Up to 5 Clones
Price: USD $ 3,600.00
Stock:
order now, ship in 3 months
abnova-minus
abnova-plus

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

    Product Description

    Mouse monoclonal antibody raised against a full-length recombinant AGA.

    Immunogen

    AGA (NP_000018.1, 1 a.a. ~ 346 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

    Sequence

    MARKSNLPVLLVPFLLCQALVRCSSPLPLVVNTWPFKNATEAAWRALASGGSALDAVESGCAMCEREQCDGSVGFGGSPDELGETTLDAMIMDGTTMDVGAVGDLRRIKNAIGVARKVLEHTTHTLLVGESATTFAQSMGFINEDLSTSASQALHSDWLARNCQPNYWRNVIPDPSKYCGPYKPPGILKQDIPIHKETEDDRGHDTIGMVVIHKTGHIAAGTSTNGIKFKIHGRVGDSPIPGAGAYADDTAGAAAATGNGDILMRFLPSYQAVEYMRRGEDPTIACQKVISRIQKHFPEFFGAVICANVTGSYGAACNKLSTFTQFSFMVYNSEKNQPTEEKVDCI

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (82); Rat (82)

    Quality Control Testing

    Antibody reactivity and specificity confirmed by ELISA and Western Blot.

    Deliverables

    Up to 5 positive hybridoma clones will be delivered to customer in the cryotube format.

    Note

    Customer should check the viability of the hybridomas within one month from the date of receipt. Fee-for-service of long term hybridoma storage can be performed upon customer's request.

  • Applications

    Western Blot (Transfected lysate)

    Western Blot (Recombinant protein)

    ELISA

  • Gene Info — AGA

    Entrez GeneID

    175

    GeneBank Accession#

    NM_000027.2

    Protein Accession#

    NP_000018.1

    Gene Name

    AGA

    Gene Alias

    AGU, ASRG, GA

    Gene Description

    aspartylglucosaminidase

    Omim ID

    208400

    Gene Ontology

    Hyperlink

    Gene Summary

    Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme. [provided by RefSeq

    Other Designations

    N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase|N4-(N-acetyl-beta-glucosaminyl)-L-asparagine amidase|aspartylglucosylamine deaspartylase|aspartylglycosaminuria|glycosylasparaginase

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