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

MEGF10 encodes a member of the multiple epidermal growth factor-like domains protein family. Additionally we are shipping MEGF10 Proteins (7) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
MEGF10 291445  
MEGF10 84466 Q96KG7
MEGF10 70417 Q6DIB5
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Top anti-MEGF10 Antibodies at antibodies-online.com

Showing 10 out of 13 products:

Catalog No. Reactivity Host Conjugate Application Quantity Supplier Delivery Price Details
Human Rabbit Alexa Fluor 555 IF (p) 100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit Alexa Fluor 647 IF (p) 100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit Biotin IHC (p), WB 100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit Alexa Fluor 488 IF (p) 100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit Alexa Fluor 350 IF (p) 100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit FITC IF (p) 100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit Alexa Fluor 594 IF (p) 100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit Cy5.5 IF (p) 100 μL Log in to see 14 to 21 Days
$379.50
Details
Human Rabbit HRP IHC (p), WB 100 μL Log in to see 14 to 21 Days
$379.50
Details
Human Rabbit Cy7 IF (p) 100 μL Log in to see 14 to 21 Days
$379.50
Details

MEGF10 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
Rat (Rattus) ,


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Human ,


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Mouse (Murine) ,


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More Antibodies against MEGF10 Interaction Partners

Human Multiple EGF-Like-Domains 10 (MEGF10) interaction partners

  1. results indicate that myogenin (show MYOG Antibodies) is a positive regulator in transcriptional regulation of MEGF10 in skeletal muscle

  2. Mutations in MEGF10 cause a recessive congenital myopathy with minicores and suggest satellite cell dysfunction as the pathogenic mechanism

  3. Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)

  4. The results of this study suggested that no association between schizophrenia and rs27388 of the MEGF10 gene in Chinese case-control sample.

  5. MEGF10 is involved in the uptake of amyloid-beta peptide (Abeta42) in the brain.

  6. in a system of forced expression by transfection, MEGF10 function can be modulated by the ATP binding cassette transporter ABCA1, ortholog to CED-7

  7. Human MEGF10 is an ortholog of Ced1 (show IFT122 Antibodies).

  8. An interaction between MEGF10 and clathrin assembly protein complex 2 medium chain (AP50 (show AP2M1 Antibodies)), a component of clathrin-coated pits was identified.

  9. In expression studies, MEGF10 had higher expression levels in the affected than the unaffected (p = .015). Schizophrenia patients with a 1/1 genotype at rs27388 had higher expressions than those patients with 1/2 and 2/2 genotypes (p = .0008).

Mouse (Murine) Multiple EGF-Like-Domains 10 (MEGF10) interaction partners

  1. studies reveal a novel role for astrocytes in mediating synapse elimination in the developing and adult brain, identify MEGF10 and MERTK (show MERTK Antibodies) as critical proteins in the synapse remodelling underlying neural circuit refinement

  2. Cysteine mutations cause defective tyrosine phosphorylation in MEGF10 myopathy.

  3. These results indicated that both Jedi-1 (show PEAR1 Antibodies) and MEGF10 can mediate phagocytosis independently through the recruitment of Syk (show SYK Antibodies).

  4. in mouse, two related transmembrane proteins, MEGF10 and MEGF11 (show MEGF11 Antibodies), have critical roles in the formation of mosaics by two retinal interneuron subtypes, starburst amacrine cells and horizontal cells

  5. Megf10 represents a novel transmembrane protein that impinges on Notch (show NOTCH1 Antibodies) signaling to regulate the satellite cell population balance between proliferation and differentiation.

MEGF10 Antigen Profile

Protein Summary

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.

Gene names and symbols associated with MEGF10

  • multiple EGF-like domains 10 (Megf10) antibody
  • multiple EGF-like-domains 10 (MEGF10) antibody
  • multiple EGF-like-domains 10 (Megf10) antibody
  • 3000002B06Rik antibody
  • EMARDD antibody
  • Gm331 antibody

Protein level used designations for MEGF10

multiple epidermal growth factor-like domains protein 10 , multiple EGF-like domains protein 10

GENE ID SPECIES
291445 Rattus norvegicus
84466 Homo sapiens
70417 Mus musculus
427126 Gallus gallus
474665 Canis lupus familiaris
100515713 Sus scrofa
539136 Bos taurus
Selected quality suppliers for anti-MEGF10 (MEGF10) Antibodies
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