CacheBy
Thermo Fisher Scientific DNMT3B Polyclonal Antibody
원본

Thermo Fisher Scientific DNMT3B Polyclonal Antibody

상품 한눈에 보기

DNMT3B 단백질을 인식하는 Rabbit Polyclonal 항체로, Human 및 Rat 시료에 반응합니다. Western blot, IHC, ICC, IP 등 다양한 응용에 사용 가능하며, 항원 친화 크로마토그래피로 정제되었습니다. PBS/glycerol buffer에 보관되며 연구용으로 적합합니다.

카탈로그번호
PA585549
판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 02. 오후 02:13
Thermo Fisher Scientific PA585549 DNMT3B Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
657,900원VAT 포함 723,690원

Thermo Fisher Scientific · Thermo Fisher Scientific DNMT3B Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:1,000–1:10,000 View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) 1:100–1:1,000 -
Immunocytochemistry (ICC/IF) 1:100–1:1,000 -
Immunoprecipitation (IP) 1:100–1:500 -

Product Specifications

Specification Description
Species Reactivity Human, Rat
Published Species Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein encompassing a sequence within the N-terminus region of human DNMT3B
Conjugate Unconjugated
Form Liquid
Concentration 1.29 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7, with 20% glycerol
Contains 0.025% ProClin 300
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_2792689

Product Specific Information

  • Keep as concentrated solution.
  • Predicted reactivity: Pig (85%).
  • Positive Control: HeLa, HeLa nuclear, GFP-tagged DNMT3B-transfected 293T.
  • Store product as a concentrated solution.
  • Centrifuge briefly prior to opening the vial.

Target Information

CpG methylation is an epigenetic modification important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have shown that DNA methylation is essential for mammalian development.
This gene encodes a DNA methyltransferase involved in de novo methylation rather than maintenance methylation. The protein localizes primarily to the nucleus and its expression is developmentally regulated.
Mutations in this gene cause immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome. Six alternatively spliced transcript variants have been described, though the full-length sequences of variants 4 and 5 have not been determined.


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

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.