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Thermo Fisher Scientific DFNA5 Polyclonal Antibody
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Thermo Fisher Scientific DFNA5 Polyclonal Antibody

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Rabbit polyclonal antibody recognizing human DFNA5 protein. Suitable for WB and IHC applications. Lyophilized form for stable storage. Reconstitute with sterile water before use. For research use only.

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pk
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마지막 업데이트 2025. 08. 03. 오전 05:01
Thermo Fisher Scientific OSD00002W-100UL DFNA5 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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563,100원VAT 포함 619,410원

Thermo Fisher Scientific · Thermo Fisher Scientific DFNA5 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:300–1:2,000
Immunohistochemistry (IHC) 1:300–1:2,000
Miscellaneous PubMed (Misc) -

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Product Specifications

Category Description
Species Reactivity Human
Published Species Not Applicable
Host / Isotype Rabbit / Ig
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide from human DFNA5 deafness (non-syndromic hearing impairment protein 5, ICERE-1) conjugated to an immunogenic carrier protein
Conjugate Unconjugated
Form Lyophilized
Concentration Not Determined
Storage Buffer Whole serum
Contains No preservative
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. Glycerol (1:1) may be added for added stability.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Reconstitute in 100 µL of sterile water. Centrifuge to remove any insoluble material.
Specificity: DFNA5.


Target Information

DFNA5 (deafness, autosomal dominant 5), also known as ICERE-1, is a 496 amino acid protein expressed in cochlea tissue, placenta, brain, heart, liver, lung, and pancreas. It exists as two alternatively spliced isoforms (short and long).
Mutations in the DFNA5 gene cause non-syndromic sensorineural deafness type 5 (DFNA5), a hereditary hearing loss condition.
The DFNA5 gene is located on human chromosome 7, which contains over 1,000 genes (~5% of the human genome). Mutations in chromosome 7 genes are associated with disorders such as Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia, and Shwachman-Diamond syndrome.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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