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Thermo Fisher Scientific TYW1 Polyclonal Antibody
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Thermo Fisher Scientific TYW1 Polyclonal Antibody

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Human TYW1 단백질을 인식하는 Rabbit Polyclonal Antibody로, WB 및 IHC(P) 실험에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, PBS 기반 버퍼에 보존됩니다. 연구용으로만 사용 가능합니다.

카탈로그번호
PA553316
판매단위
pk
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마지막 업데이트 2025. 07. 27. 오전 02:22
Thermo Fisher Scientific PA553316 TYW1 Polyclonal Antibody 100 ul pk판매 단위 pk
재고 1개
773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific TYW1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:20–1:50

Product Specifications

항목 내용
Species Reactivity Human
Host/Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human TYW1. Recombinant protein control fragment (Product # RP-90614)
Conjugate Unconjugated
Form Liquid
Concentration 0.05 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_2649152

Product Specific Information

Immunogen sequence:
RRAMITPALR EALTKQGYQL IGSHSGVKLC RWTKSMLRGR GGCYKHTFYG IESHRCMETT PSLACANKCV FCWRHHTNPV GTEWRWKMDQ PEMILKEAIE NHQNMIKQFK GVPGVKA

Antigen sequence identity:

  • Mouse: 97%
  • Rat: 96%

Target Information

TYW1 (also known as TYW1A, RSAFD1, or YPL207W) is a 732 amino acid protein containing one flavodoxin-like domain that participates in the wybutosine-tRNA (Phe) biosynthesis pathway.
Wybutosine (yW) is a hypermodified guanosine at the 3′ position adjacent to the anticodon of phenylalanine tRNA that stabilizes codon-anticodon interactions during decoding on the ribosome.
TYW1 is involved in a multistep enzymatic reaction that stabilizes codon-anticodon base-pairing during ribosomal decoding, ensuring correct translation.
It binds one 4Fe-4S cluster and is located on human chromosome 7.
Defects in genes on chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Lissencephaly, Citrullinemia, and Shwachman-Diamond syndrome, suggesting that TYW1 may play a role in these conditions.


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

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