Date published: 2025-9-11

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O-GlcNAc 항체 (CTD110.6): sc-59623

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데이터 시트
  • O-GlcNAc 항체 CTD110.6 는 마우스 monoclonal IgM κ O-GlcNAc 항체, 71간행물에 인용, 이며 200 µg/ml으로 제공합니다.
  • 세린-O-결합 N-아세틸글루코사민을 함유한 O-GlcNAc에 대해 양성 반응
  • WB와 IP으로 a broad range of species, including mammals, insects, worms, plants와 filamentous fungi origin의 Ser-O-GlcNAc and Thr-O-GlcNAc을 검출할것을 권장합니다.; peptide determinants or other closely-related carbohydrate antigens와 교차반응이 없습니다.
  • See O-GlcNAc (RL2): sc-59624 for additional antibody conjugates, including AC, HRP, FITC, PE, Alexa Fluor® 488, 594, 647, 680 and 790.
  • O-GlcNAc (CTD110.6): sc-59623무료10 µg 샘플을 신청하려면 기술지원팀 (또는 로컬 디스트리뷰터)에 연락주세요.
  • 현재 O-GlcNAc 항체(CTD110.6)에 대해 선호하는 2차 검출 시약의 식별을 아직 완료하지 못했습니다. 이 작업은 진행 중입니다.

빠른 링크

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O-GlcNAc 항체 (CTD110.6)는 IgM κ 마우스 단일클론 O-GlcNAc 항체 (O-linked β-N-아세틸글루코사민 항체, O-β-GlcNAc 항체, O-linked GlcNAc 항체, 세린 하이드록실 O-GlcNAc 항체, 트레오닌 하이드록실 O-GlcNAc 항체 또는 O-GlcNAcylation 특이 항체)로 WB 및 IP에 의한 포유류, 곤충, 벌레, 식물 및 사상균을 포함한 광범위한 종의 O-GlcNAc 단백질을 검출한다. O-GlcNAc 항체 (CTD110.6)는 비-접합 항-O-GlcNAc 항체로 사용할 수 있다. O-GlcNAc (O-linked N-아세틸글루코사민)는 진핵 세포의 핵 및 세포질에서만 발견되는 단백질 글리코실화의 한 형태이다. 많은 단백질은 O-GlcNAc의 부착에 의해 세린 및 트레오닌 하이드록실 그룹에서 변형된다. 핵 기공 안팎의 인신매매를 조절하는 단백질은 광범위하게 O-GlcNAcylated된다. 인산화된 O-GlcNAc 단백질은 다른 단백질과 가역적인 다중 복합체를 형성하며 이러한 연관성은 종종 인산화에 의해 조절된다. O-GlcNAc 단백질은 종양 및 다양한 암 세포의 병리 발생에 중요한 역할을 할 수 있다. O-GlcNAc 잔기는 사전 개시 복합체의 조립을 조절하므로 전사 개시에 중요하다. 세포골격 및 막 O-GlcNAc 단백질은 적혈구 세포 모양을 유지하고 알츠하이머병의 병변을 담당하는 단백질의 분해를 조절한다.

연구용으로만 사용가능합니다. 진단이나 치료용으로 사용불가합니다.

Alexa Fluor®는 미국 오리건주 Molecular Probes Inc.의 상표입니다.

LI-COR®와 Odyssey®는 LI-COR Biosciences의 등록 상표입니다.

O-GlcNAc 항체 (CTD110.6) 참고문헌:

  1. O-GlcNAc 전이 효소 유전자는 X 염색체에 존재하며 배아 줄기세포의 생존력과 생쥐의 발생에 필수적인 역할을 합니다.  |  Shafi, R., et al. 2000. Proc Natl Acad Sci U S A. 97: 5735-9. PMID: 10801981
  2. 쥐 소뇌 피질에서 O-GlcNAc 전이 효소 및 O-GlcNAc 변형 단백질의 국소화.  |  Akimoto, Y., et al. 2003. Brain Res. 966: 194-205. PMID: 12618343
  3. 핵 및 세포질 단백질의 글리코실화. 우리딘 디포스포-N-아세틸글루코사민:폴리펩타이드 베타-N-아세틸글루코사미닐전달효소의 정제 및 특성 분석.  |  Haltiwanger, RS., et al. 1992. J Biol Chem. 267: 9005-13. PMID: 1533623
  4. 매두 바이러스 감염에 관여하는 O-GlcNAc 전이 효소로 비밀 에이전트를 확인했습니다.  |  Chen, D., et al. 2005. J Virol. 79: 9381-7. PMID: 16014901
  5. O-GlcNAc 전이 효소에 대한 고처리량 분석은 펩타이드 기질에서 주요 서열 선호도를 감지합니다.  |  Leavy, TM. and Bertozzi, CR. 2007. Bioorg Med Chem Lett. 17: 3851-4. PMID: 17531489
  6. 포스포이노시타이드 신호는 O-GlcNAc 전이효소와 인슐린 저항성을 연결합니다.  |  Yang, X., et al. 2008. Nature. 451: 964-9. PMID: 18288188
  7. PPARβ/δ-orchestrated metabolic reprogramming은 기억 CD8+ T 세포의 형성과 유지를 돕습니다.  |  Ju Kim, E. 2020. Chembiochem. 21: 3026-3035. PMID: 32406185
  8. 단백질 O-GlcNAc 글리코실화 반응의 화학적 프로빙의 발전: 구조적 역할과 분자 메커니즘.  |  Saha, A., et al. 2021. Chem Soc Rev. 50: 10451-10485. PMID: 34338261
  9. 스트레스 반응 경로에 O-GlcNAc의 통합.  |  Fahie, KMM., et al. 2022. Cells. 11: PMID: 36359905
  10. GSDMD의 O-GlcNAc 변형은 LPS에 의해 유발된 내피 세포의 파이로토시스(pyroptosis)를 약화시킵니다.  |  Yu, F., et al. 2024. Inflamm Res. 73: 5-17. PMID: 37962578
  11. 핵 및 세포질 단백질의 동적 글리코실화. 여러 개의 테트라트리코펩타이드 반복을 가진 고유한 O-GlcNAc 전이 효소의 복제 및 특성 분석.  |  Kreppel, LK., et al. 1997. J Biol Chem. 272: 9308-15. PMID: 9083067
  12. O-연결 GlcNAc 전이효소는 4중사슬 펩타이드 반복을 포함하는 보존된 핵세포질 단백질입니다.  |  Lubas, WA., et al. 1997. J Biol Chem. 272: 9316-24. PMID: 9083068

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O-GlcNAc 항체 (CTD110.6)

sc-59623
200 µg/ml
RMB2377.00

I need specifically detect O-GlcNAcylation un plant proteim extractos. We found lack of specificity using CTD110.6. Employment of a secondary anti-IgM is mandatory? It could be conveniente to use RL2?

Asked by: Salamandra
Thank you for your question. It would be helpful if you could call us, allowing for a more interactive discussion of this and other related questions.
Answered by: Technical Support
Date published: 2021-07-23

I am planning to IP this modification after protein digestion to peptides and wonder if the antibody recognise digested peptides carrying this modifications and if you would expect some specificity for certain peptides?

Asked by: Paolo
Thank you for your question. Unfortunately I do not have any information regarding if this antibody can detect digested peptides.
Answered by: Tech Service
Date published: 2019-04-09

What is the best way to avoid background when working on mouse samples with this mouse monoclonal antibody?

Asked by: AbPolly
Thank you for your inquiry. Our new line of Mouse IgG binding proteins can help reduce non-specific staining with mouse samples. A complete list of available binding proteins is available on our website here: https://www.scbt.com/scbt/browse/support-products-mouse-igg-binding-proteins/_/N-ecrety You can also use our alternative O-GlcNAc antibody sc-59624 in a variety of direct conjugations to reduce non-specific staining with mouse samples.
Answered by: Technical Service
Date published: 2016-12-22
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Rated 5 out of 5 by from goodvery nice,it work well in WB。Good specificity,nonspecific bands
Date published: 2021-07-31
Rated 4 out of 5 by from clear signal in immunofluorescence, dirty in WBThis antibody worked well in immunofluorescence in cell culture and also in paraffin embedded human brain tissue. In western blot, it needs a lot of washes after primary antibody especially, usually the first time there's a dark smear everywhere and if exposure is less than 5 min there's no signal. Usually after re-application of the secondary the signal gets clearer, perhaps due to longer washing of primary. Primary seems to stick, but this is a problem of this clone, not of this product in particular. Here are the captions again for the vertical (tissue) and horizontal (cells) IF pictures and the western blot since they did not fit in the space given: Cells: Immunofluorescence for O-GlcNAc in human astrocytes. A) no primary antibody. B) DMSO treatment (control). C) 200 uM Voc OGT inhibitor treatment. D) 100 uM 9D OGA inhibitor treatment. Green: O-GlcNAc (Santa Cruz CTD110.6), Blue: DAPI. Primary antibody was used at 1:100 dilution overnight in 5% goat serum in PBS. Secondary antibody was Goat anti-mouse IgM Alexafluor 488 conjugate. Tissue: Immunofluorescence in human tissue. A) IF of formalin fixed paraffin embedded human brain tissue. Control patient in his 60s. B) Alzheimer’s disease patient in his 60s. Green: O-GlcNAc. Blue: DAPI. Tissues were reparaffinized, rehydrated, antigen retrieval was performed in boiling citrate buffer, free formaldehydes were blocked with sodium borohydride. Blocking and antibody incubations were done in 5% goat serum in PBS. Lipofuscin was blocked with Sudan black for 20 min. after DAPI incubation. Western blot: Western blot with human astrocyte lysates. Multiple samples were run on SDS-PAGE gels and transferred to PVDF membrane. Blocking was with 5% milk in TBST. Primary antibody was used at 1:100 dilution in 5% BSA in TBST. Secondary antibody (rabbit anti-mouse IgM HRP) was diluted 1:1000 in 5% milk in TBST. Membrane was washed 2x 5 mins then 30 min in TBST after primary and then 3x 5 min after secondary. Imaging was for 10 mins.
Date published: 2020-12-30
Rated 5 out of 5 by from good result do WBWe used this antibody recenlty and following the struction choose the dilution 1:400(we feel it can diluted more),the band is right size,very good result.
Date published: 2018-05-26
Rated 4 out of 5 by from Worked wellI bought antibody for pilot experiments and it woked well in Western. I will be happy to buy more for future work.
Date published: 2018-02-16
Rated 5 out of 5 by from Really good !I used this antibody several times. It works well on human lung cells. even using a low dilution
Date published: 2017-07-05
Rated 5 out of 5 by from Great for Western blotMonoclonal O-GlcNAc (CTD110.6) antibody has been validated by Western blot. Highly recommended!
Date published: 2016-12-19
Rated 5 out of 5 by from Publishable WBPublishable WB.CoIP data with rat aortic smooth muscle cells - SCBT Publication Review
Date published: 2015-04-10
Rated 4 out of 5 by from Dirty blot but produced bands at expectedDirty blot but produced bands at expected MW in HeLa nuclear extract and A549 whole cell lysate and mouse brain tissue extract. -SCBT QC
Date published: 2015-03-26
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O-GlcNAc 항체 (CTD110.6) is rated 4.7 out of 5 by 10.
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