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FRAS1

Fraser Syndrome 1

FRAS1 encodes an extracellular matrix protein that appears to function in the regulation of epidermal-basement membrane adhesion and organogenesis during development. Mutations in this gene cause Fraser syndrome, a multisystem malformation that can include craniofacial, urogenital and respiratory system abnormalities. Alternative splicing results in multiple transcript variants.

Gene Name: Fraser Syndrome 1
Synonyms: FRAS1, Fraser syndrome 1, KIAA1500
Target Sequences: NM_025074

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Antibodies (1)
Primary (1)
FRAS1 (1)
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rabbit (1)
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polyclonal pc (1)
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aa3025-3075 (1)
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FRAS1 Antibody - Detection of human FRAS1 by western blot. Samples: Whole cell lysate (50 µg) from HeLa, HEK293T, and Jurkat cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-FRAS1 antibody used for WB at 1:1000. Detection: Chemiluminescence with an exposure time of 3 minutes.
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FRAS1 Rabbit anti-Human Polyclonal (aa3025-3075) Antibody
Human
IP, WB
Unconjugated
10 µl/$295
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If you do not find the reagent or information you require, please contact Customer.Support@LSBio.com to inquire about additional products in development.

PLEASE NOTE

For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).