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Thermo Fisher Scientific ZNF408 Polyclonal Antibody
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Thermo Fisher Scientific ZNF408 Polyclonal Antibody

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Human ZNF408 단백질을 인식하는 Rabbit Polyclonal 항체로, IHC(P)에서 1:50–1:200 희석 비율로 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol buffer에 보관. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 03. 오전 12:37
Thermo Fisher Scientific PA553660 ZNF408 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific ZNF408 Polyclonal Antibody

Applications and Tested Dilution

  • 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 ZNF408. Recombinant protein control fragment (Product #RP-91666)
Conjugate Unconjugated
Form Liquid
Concentration 0.2 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_2650107

Product Specific Information

Immunogen sequence:
AAVAVVTEVE SAVQQEVASP GEDAAEPCID PGSQSPSGIQ AENMVSPGLK FPTQDRISKD SQPLGPLLQD GDVDEECPAQ AQMPPELQSN SATQQDPDGS GASFSSSARG TQPHGYLAKK LHSPSDQCPP RAKTPEPGAQ QSGFPTLSRS

Highest antigen sequence identity to the following orthologs:

  • Mouse: 40%
  • Rat: 25%

Target Information

Zinc-finger proteins contain DNA-binding domains and have diverse functions in transcriptional activation or repression. Most zinc-finger proteins include a Kruppel-type DNA binding domain and a KRAB domain, which interacts with KAP1 to recruit histone-modifying proteins.
ZNF408, a member of the Kruppel C2H2-type zinc-finger protein family, is encoded on human chromosome 11, which contains over 1,400 genes and represents nearly 4% of the human genome. Mutations in genes on chromosome 11 are associated with disorders such as Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema, and Smith-Lemli-Opitz syndrome.


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

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