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Thermo Fisher Scientific DFNA5 Monoclonal Antibody (A1H2)
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Thermo Fisher Scientific DFNA5 Monoclonal Antibody (A1H2)

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DFNA5 단백질을 인식하는 Thermo Fisher Scientific의 Mouse Monoclonal Antibody (A1H2). Western blot, ICC/IF, Flow cytometry에 최적화. Human 시료 반응성, Protein G 정제, 고농도(2 mg/mL) 액상 형태로 안정적 보관 가능.

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마지막 업데이트 2025. 08. 05. 오전 10:50
Thermo Fisher Scientific MA537799 DFNA5 Monoclonal Antibody (A1H2) 100 ul pk판매 단위 pk ·
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655,000원VAT 포함 720,500원

Thermo Fisher Scientific · Thermo Fisher Scientific DFNA5 Monoclonal Antibody (A1H2)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunocytochemistry (ICC/IF) 1:50–1:100
Flow Cytometry (Flow) 1:50–1:100

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone A1H2
Immunogen Recombinant protein within Human DFNA5 (aa 34–214)
Conjugate Unconjugated
Form Liquid
Concentration 2 mg/mL
Purification Protein G
Storage Buffer PBS, pH 7.4, with 0.2% BSA, 50% glycerol
Contains 0.05% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2897723

Product Specific Information

Positive controls: Hela cell lysates, HepG2 cell lysates, A431, SiHa, SH-SY5Y.


Target Information

DFNA5 (deafness, autosomal dominant 5), also known as ICERE-1, is a 496 amino acid protein expressed in cochlea tissue as well as placenta, brain, heart, liver, lung, and pancreas. It exists as two alternatively spliced isoforms (short and long). Mutations in DFNA5 cause non-syndromic sensorineural deafness autosomal dominant type 5 (DFNA5), a form of hearing loss due to damage in auditory structures.
The DFNA5 gene is located on human chromosome 7, which contains over 1,000 genes and represents nearly 5% of the human genome. Defects in genes on chromosome 7 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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