CacheBy
Thermo Fisher Scientific ZDHHC16 Polyclonal Antibody
원본

Thermo Fisher Scientific ZDHHC16 Polyclonal Antibody

상품 한눈에 보기

ZDHHC16 단백질을 인식하는 Thermo Fisher Scientific의 토끼 폴리클로날 항체. Western blot 및 IHC(P)에서 검증됨. 항원 친화 크로마토그래피로 정제되어 순도 95% 이상. 인간, 마우스, 랫트 반응성. 연구용으로 사용.

카탈로그번호
PA577176
판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 05. 오후 05:40
Thermo Fisher Scientific PA577176 ZDHHC16 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
731,200원VAT 포함 804,320원

Thermo Fisher Scientific · Thermo Fisher Scientific ZDHHC16 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant full length Human ZDHHC16
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage buffer PBS with 50% glycerol
Contains 0.02% sodium azide
Storage conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions Wet ice
RRID AB_2720903

Product Specific Information

The antibody was affinity-purified from rabbit antiserum by affinity chromatography using an epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.

Target Information

ZDHHC16 (zinc finger, DHHC-type containing 16), also known as APH2, is a 377-amino-acid multi-pass membrane protein localized to the endoplasmic reticulum and containing one DHHC-type zinc finger. It exists as multiple alternatively spliced isoforms, interacts with c-Abl, and catalyzes the conversion of Palmitoyl-CoA and protein-cysteine to S-palmitoyl protein and CoA. Through its association with c-Abl, ZDHHC16 may be involved in regulating apoptosis. The gene encoding ZDHHC16 maps to human chromosome 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. Mutations in genes on chromosome 10 are associated with several disorders, including Charcot-Marie-Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2, and porphyria.

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.