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Thermo Fisher Scientific DKC1 Polyclonal Antibody
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Thermo Fisher Scientific DKC1 Polyclonal Antibody

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Rabbit 유래 DKC1 폴리클로날 항체로 Western blot과 Immunoprecipitation에 적합. Human DKC1의 340–390번 잔기 영역을 항원으로 사용. Mouse, Rat, D. melanogaster, Chicken과 반응 예측. 연구용으로만 사용 가능.

카탈로그번호
A302591Ax (2개 옵션)
판매단위
pk
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2개 옵션
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마지막 업데이트 2025. 08. 05. 오후 05:00
Thermo Fisher Scientific A302591AM DKC1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
477,300원VAT 포함 525,030원
Thermo Fisher Scientific A302591AT DKC1 Polyclonal Antibody 10 ul pk판매 단위 pk ·
재고 확인 필요
194,600원VAT 포함 214,060원

Thermo Fisher Scientific · Thermo Fisher Scientific DKC1 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:2,000–1:10,000

Immunoprecipitation (IP)

  • Tested Dilution: 5–15 µg/mg lysate

Product Specifications

항목 내용
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Region between residue 340 and 390 of human dyskeratosis congenita 1
Conjugate Unconjugated
Form Liquid
Concentration 0.20 mg/mL
Storage Conditions 4°C
Shipping Conditions Wet ice

Product Specific Information

  • Recommended shelf life: 1 year from date of receipt
  • Based on 100% sequence identity, this antibody is predicted to react with Mouse, Rat, D. melanogaster, and Chicken

Target Information

This gene is a member of the H/ACA snoRNPs gene family. snoRNPs are involved in various aspects of rRNA processing and modification and have been classified into two families: C/D and H/ACA.
The H/ACA snoRNPs also include the NOLA1, 2, and 3 proteins. The protein encoded by this gene and the three NOLA proteins localize to the dense fibrillar components of nucleoli and to coiled bodies in the nucleus.
Both 18S rRNA production and rRNA pseudouridylation are impaired if any one of the four proteins is depleted. These four H/ACA snoRNP proteins are also components of the telomerase complex.
The protein encoded by this gene is related to the Saccharomyces cerevisiae Cbf5p and Drosophila melanogaster Nop60B proteins.
The gene lies in a tail-to-tail orientation with the palmitoylated erythrocyte membrane protein gene and is transcribed in a telomere-to-centromere direction.
Both nucleotide substitutions and single trinucleotide repeat polymorphisms have been found in this gene.
Mutations in this gene cause X-linked dyskeratosis congenita, a disease resulting in reticulate skin pigmentation, mucosal leukoplakia, nail dystrophy, and progressive bone marrow failure.
Mutations also cause Hoyeraal-Hreidarsson syndrome, a more severe form of dyskeratosis congenita.
Two transcript variants encoding different isoforms have been found for this gene.

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

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