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MEGF10 antibody (AA 26-160)

The Rabbit Polyclonal anti-MEGF10 antibody has been validated for WB. It is suitable to detect MEGF10 in samples from Human.
Catalog No. ABIN6143719

Quick Overview for MEGF10 antibody (AA 26-160) (ABIN6143719)

Target

See all MEGF10 Antibodies
MEGF10 (Multiple EGF-Like-Domains 10 (MEGF10))

Reactivity

  • 18
  • 13
  • 2
Human

Host

  • 29
Rabbit

Clonality

  • 29
Polyclonal

Conjugate

  • 6
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MEGF10 antibody is un-conjugated

Application

  • 14
  • 13
  • 10
  • 5
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 8
    • 3
    • 1
    • 1
    AA 26-160

    Sequence

    LNLEDPNVCS HWESYSVTVQ ESYPHPFDQI YYTSCTDILN WFKCTRHRVS YRTAYRHGEK TMYRRKSQCC PGFYESGEMC VPHCADKCVH GRCIAPNTCQ CEPGWGGTNC SSACDGDHWG PHCTSRCQCK NGALC

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 26-160 of human MEGF10 (NP_001295048.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Comment

    HIGH QUALITY

    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

    MEGF10 (Multiple EGF-Like-Domains 10 (MEGF10))

    Alternative Name

    MEGF10

    Background

    This gene encodes a member of the multiple epidermal growth factor-like domains protein family. The encoded protein plays a role in cell adhesion, motility and proliferation, and is a critical mediator of apoptotic cell phagocytosis as well as amyloid-beta peptide uptake in the brain. Expression of this gene may be associated with schizophrenia, and mutations in this gene are a cause of early-onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD) as well as congenital myopathy with minicores. Alternatively spliced transcript variants have been observed for this gene.,MEGF10,EMARDD,Cell Biology & Developmental Biology,Apoptosis,Endocrine & Metabolism,Stem Cells,Mesenchymal Stem Cells,MEGF10

    Molecular Weight

    60 kDa/122 kDa

    Gene ID

    84466

    UniProt

    Q96KG7

    Pathways

    Regulation of Muscle Cell Differentiation
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