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anti-Family with Sequence Similarity 58, Member B (FAM58B) Antibodies

Mutations in FAM58B have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations.

list all antibodies Gene Name GeneID UniProt
FAM58B 92002 Q8N1B3
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Top anti-Family with Sequence Similarity 58, Member B Antibodies at antibodies-online.com

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Catalog No. Reactivity Host Conjugate Application Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated IHC, ELISA, WB 100 μg Log in to see 5 to 6 Days
$485.80
Details

FAM58B Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality
Human


More Antibodies against Family with Sequence Similarity 58, Member B Interaction Partners

Human Family with Sequence Similarity 58, Member B (FAM58B) interaction partners

  1. Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations.

Family with Sequence Similarity 58, Member B (FAM58B) Antigen Profile

Protein Summary

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Gene names and symbols associated with FAM58B

  • family with sequence similarity 58, member A (FAM58A) antibody
  • STAR antibody

Protein level used designations for FAM58B

cyclin M , cyclin-related protein FAM58A

GENE ID SPECIES
92002 Homo sapiens
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