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Thermo Fisher Scientific ZDHHC16 Polyclonal Antibody
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Thermo Fisher Scientific ZDHHC16 Polyclonal Antibody

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Human ZDHHC16 단백질을 인식하는 Rabbit Polyclonal 항체로, Western blot 및 IHC(P) 실험에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol 완충액에 보존됩니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 05. 오전 08:54
Thermo Fisher Scientific PA558965 ZDHHC16 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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876,300원VAT 포함 963,930원

Thermo Fisher Scientific · Thermo Fisher Scientific ZDHHC16 Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human ZDHHC16. Recombinant protein control fragment (Product # RP-91045)
Conjugate Unconjugated
Form Liquid
Concentration 0.1 mg/mL
Purification Antigen affinity chromatography
Storage buffer PBS, pH 7.2, with 40% 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_2649853

Product Specific Information

Immunogen sequence:
VLISRGETSI ERHINKKERR RLQAKGRVFR NPYNYGCLDN WKVFLGVDTG RHWLTRVLLP SSHLPHGNGM SWEPPPWVTA

Highest antigen sequence identity to the following orthologs:

  • Mouse: 99%
  • Rat: 99%

Target Information

ZDHHC16 (zinc finger, DHHC-type containing 16), also known as APH2, is a 377 amino acid multi-pass membrane protein that localizes to the endoplasmic reticulum and contains one DHHC-type zinc finger. Existing as multiple alternatively spliced isoforms, ZDHHC16 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 the regulation of 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. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic 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.

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