CacheBy
Thermo Fisher Scientific DFNA5 Polyclonal Antibody
원본

Thermo Fisher Scientific DFNA5 Polyclonal Antibody

상품 한눈에 보기

Human DFNA5 단백질을 인식하는 Rabbit Polyclonal 항체로, WB, IHC(P), Flow Cytometry에 사용 가능. 1 mg/mL 농도의 액상 형태이며, Affinity chromatography로 정제됨. PBS buffer(50% glycerol, 0.2% BSA)로 보존되며 -20°C 보관 권장.

판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 04. 오후 05:49
Thermo Fisher Scientific PA5109333 DFNA5 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
595,300원VAT 포함 654,830원

Thermo Fisher Scientific · Thermo Fisher Scientific DFNA5 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Flow Cytometry (Flow) 1:50–1:100

Product Specifications

Specification Detail
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein within Human DFNA5/GSDME aa 1–220
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4, with 50% glycerol, 0.2% BSA
Contains 0.05% sodium azide
Storage Conditions -20°C, avoid freeze/thaw cycles, store in dark
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2854744

Product Specific Information

Positive Control:
SiHa cell lysates, rat testis tissue, human thyroid gland tissue, human breast tissue, mouse small intestine tissue.

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 as two alternatively spliced isoforms (short and long).
Defects in the DFNA5 gene cause non-syndromic sensorineural deafness autosomal dominant type 5 (DFNA5), a form of hearing loss resulting from damage to sound-receiving structures in the brain.
The DFNA5 gene is located on human chromosome 7, which contains over 1,000 genes and represents nearly 5% of the human genome. Mutations 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.

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.