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anti-Family with Sequence Similarity 83, Member H (FAM83H) Antibodies

The protein encoded by FAM83H plays an important role in the structural development and calcification of tooth enamel. Additionally we are shipping and FAM83H Kits (1) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
FAM83H 286077 Q6ZRV2
FAM83H 105732 Q148V8
FAM83H    
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Top anti-FAM83H Antibodies at antibodies-online.com

Showing 4 out of 5 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated WB HL-60 lysate probed with Rabbit Anti-FAM83H Polyclonal Antibody, Unconjugated  at 1:5000 for 90min at 37˚C. 100 μL Log in to see 3 to 7 Days
$269.50
Details
Human Rabbit Biotin WB   100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit HRP WB   100 μL Log in to see 14 to 21 Days
$379.50
Details
Human Rabbit Un-conjugated IP, WB   100 μL Log in to see 8 to 10 Days
$595.83
Details

FAM83H Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
Human ,


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Mouse (Murine)


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Rat (Rattus)


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More Antibodies against FAM83H Interaction Partners

Human Family with Sequence Similarity 83, Member H (FAM83H) interaction partners

  1. FAM83H missense mutation reported in one of the 3 Chilean families analyzed in this study might cause a phenotype of hypocalcified enamel more attenuated with retention of amelogenin (show AMELX Antibodies).

  2. In hereditary amelogenesis imperfect, our study demonstrates that FAM83H mutations could influence enamel biomineralization and dentine formation.

  3. Results suggest keratin cytoskeleton organization is regulated by FAM83H recruitment of CK-1alpha to keratins, and keratin filament disassembly caused by overexpression of FAM83H and localization of CK-1alpha contribute to the progression of colorectal cancer.

  4. amelogenesis imperfecta-causing mutations were identified in three of the probands: 3)a previously described nonsense transition mutation in a single allele of FAM83H (c.1379G>A; g.5663G>A; p.W460*)

  5. Mutations in FAM83H and ENAM (show ENAM Antibodies) and related phenotypes were observed in Chinese families with amelogenesis imperfecta.

  6. This study reports on a novel FAM83H nonsense mutation, p.Y302X, in a Danish five-generation family with autosomal dominant hypocalcified amelogenesis imperfect. The phenotypic variation in the affected family members with this mutation was limited.

  7. nuclear targeting of the truncated FAM83H protein contributes to the severe, generalized enamel phenotype in [autosomal-dominant hypocalcification amelogenesis imperfecta]

  8. the C-terminal portion of FAM83H is required for tooth enamel calcification

  9. a novel nonsense FAM83H mutation (c.1374C 1 A; p.Y458X)causing autosomal dominant hypocalcified amelogenesis imperfecta

  10. FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta demonstrate that FAM83H is required for proper dental-enamel calcification.

Mouse (Murine) Family with Sequence Similarity 83, Member H (FAM83H) interaction partners

  1. Findings demonstrate that over-expression of FAM83H in mice does not produce a phenotype in dentine or enamel.

FAM83H Antigen Profile

Protein Summary

The protein encoded by this gene plays an important role in the structural development and calcification of tooth enamel. Defects in this gene are a cause of amelogenesis imperfecta type 3 (AI3).

Gene names and symbols associated with FAM83H

  • family with sequence similarity 83, member H (FAM83H) antibody
  • family with sequence similarity 83, member H (Fam83h) antibody
  • si:ch211-199g17.1 (si:ch211-199g17.1) antibody
  • AA409316 antibody
  • AI3 antibody
  • fa03f11 antibody
  • fam83h antibody
  • wu:fa03f11 antibody

Protein level used designations for FAM83H

FAM83H variant 1 , protein FAM83H

GENE ID SPECIES
286077 Homo sapiens
105732 Mus musculus
565918 Danio rerio
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