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Thermo Fisher Scientific SCYL1 Polyclonal Antibody
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Thermo Fisher Scientific SCYL1 Polyclonal Antibody

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SCYL1 단백질을 인식하는 Thermo Fisher Scientific의 토끼 폴리클로날 항체로, 인간 시료에 반응합니다. ICC/IF에 적합하며 항원 친화 크로마토그래피로 정제되었습니다. 0.2 mg/mL 농도의 액상 형태로 제공되며, 4°C 단기 보관 및 -20°C 장기 보관이 가능합니다.

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마지막 업데이트 2025. 08. 04. 오전 08:43
Thermo Fisher Scientific PA553267 SCYL1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific SCYL1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human SCYL1. Recombinant protein control fragment (Product # RP-91451)
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_2647042

Product Specific Information

Immunogen sequence:

AFPEDFCRHK VLPQLLTAFE FGNAGAVVLT PLFKVGKFLS AEEYQQKIIP VVVKMFSSTD
RAMRIRLLQQ MEQFIQYLDE PTVNTQIFPH VVHGFLDTNP AIREQTVKSM LLLAPKLNEA NLNVELMK

Sequence identity with orthologs:

  • Mouse: 96%
  • Rat: 95%

Target Information

Chromosome 11 contains approximately 135 million base pairs and around 1,400 genes, representing about 4% of human genomic DNA. It is considered gene- and disease-association dense. The Atm gene on chromosome 11 is critical for regulating cell cycle arrest and apoptosis following double-strand DNA breaks. Mutations in Atm cause ataxia-telangiectasia.
Other notable genes include:

  • HBB: mutations cause Sickle cell anemia and β-thalassemia
  • WT1: mutations associated with Wilms’ tumor, WAGR syndrome, and Denys-Drash syndrome
  • Additional disorders linked to chromosome 11 include 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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