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Thermo Fisher Scientific TDG Polyclonal Antibody, MaxPab
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Thermo Fisher Scientific TDG Polyclonal Antibody, MaxPab

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TDG 단백질을 인식하는 Thermo Fisher Scientific의 다클론 항체로, Western blot 및 Immunocytochemistry에 적합합니다. 인간 단백질 반응성을 가지며, 액상 형태로 제공됩니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 05. 오후 09:20
Thermo Fisher Scientific H00006996-B01P TDG Polyclonal Antibody, MaxPab 50 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

Thermo Fisher Scientific · Thermo Fisher Scientific TDG Polyclonal Antibody, MaxPab

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:1,000

Immunocytochemistry (ICC/IF)

  • Tested Concentration: 10 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG
Class Polyclonal
Type Antibody
Immunogen TDG (AAH37557.1, 1–410 a.a.) full-length human protein
Conjugate Unconjugated
Form Liquid
Concentration See Label
Purification Affinity chromatography
Storage buffer PBS, pH 7.4
Contains No preservative
Storage conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Sequence of this protein is as follows:
MEAENAGSYS LQQAQAFYTF PFQQLMAEAP NMAVVNEQQM PEEVPAPAPA QEPVQEAPKG RKRKPRTTEP KQPVEPKKPV ESKKSGKSAK SKEKQEKITD TFKVKRKVDR FNGVSEAELL TKTLPDILTF NLDIVIIGIN PGLMAAYKGH HYPGPGNHFW KCLFMSGLSE VQLNHMDDHT LPGKYGIGFT NMVERTTPGS KDLSSKEFRE GGRILVQKLQ KYQPRIAVFN GKCIYEIFSK EVFGVKVKNL EFGLQPHKIP DTETLCYGMP SSSARCAQFP RAQDKVHYYI KLKDLRDQLK GIERNMDVQE VQYTFDLQLA QEDAKKMAVK EEKYDPGYEA AYGGAYGENP CSSEPCGFSS NGLIESVELR GESAFSGIPN GQWMTQSFTD QIPSFSNHCG TQEQEEESHA

Target Information

The protein encoded by this gene belongs to the TDG/mug DNA glycosylase family.
Thymine-DNA glycosylase removes thymine moieties from G/T mismatches by hydrolyzing the carbon-nitrogen bond between the DNA backbone and mispaired thymine.
With lower activity, it also removes thymine from C/T and T/T mispairings, as well as uracil and 5-bromouracil from mispairings with guanine.
TDG plays a central role in cellular defense against genetic mutations caused by spontaneous deamination of 5-methylcytosine and cytosine.
This gene may have a pseudogene in the p arm of chromosome 12.


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

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