MMADHC mouse monoclonal antibody (hybridoma)

Catalog # H00027249-M

Size

Price

Stock

Quantity

Size:Up to 5 Clones
Price: USD $ 3,600.00
Stock:
order now, ship in 3 months
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

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

    Immunogen

    MMADHC (NP_056517.1, 1 a.a. ~ 296 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

    Sequence

    MANVLCNRARLVSYLPGFCSLVKRVVNPKAFSTAGSSGSDESHVAAAPPDICSRTVWPDETMGPFGPQDQRFQLPGNIGFDCHLNGTASQKKSLVHKTLPDVLAEPLSSERHEFVMAQYVNEFQGNDAPVEQEINSAETYFESARVECAIQTCPELLRKDFESLFPEVANGKLMILTVTQKTKNDMTVWSEEVEIEREVLLEKFINGAKEICYALRAEGYWADFIDPSSGLAFFGPYTNNTLFETDERYRHLGFSVDDLGCCKVIRHSLWGTHVVVGSIFTNATPDSHIMKKLSGN

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (93); Rat (92)

    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 — MMADHC

    Entrez GeneID

    27249

    GeneBank Accession#

    NM_015702.1

    Protein Accession#

    NP_056517.1

    Gene Name

    MMADHC

    Gene Alias

    C2orf25, CL25022

    Gene Description

    methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X

    Other Designations

    protein C2orf25, mitochondrial

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