생물학적 소스
goat
결합
unconjugated
항체 형태
affinity isolated antibody
항체 생산 유형
primary antibodies
클론
polyclonal
양식
buffered aqueous solution
종 반응성
canine, human, mouse, pig, bovine
기술
indirect ELISA: suitable
western blot: suitable
UniProt 수납 번호
배송 상태
dry ice
저장 온도
−20°C
유전자 정보
human ... ZRANB1(54764)
일반 설명
Zinc finger RANBP2-type containing 1 (ZRANB1) is a deubiquitinase which is part of the OTU family. It possesses an ovarian tumor (OTU) catalytic domain. This 708 amino acid protein consists of three amino-terminal Npl4-like zinc finger (NZF) domains. The ZRANB1 gene is localized on human chromosome 10q26.13.
면역원
Peptide with sequence KWLDRYRQIRPCTS from the C Terminus of the protein sequence according to NP_060050.2.
생화학적/생리학적 작용
Zinc finger RANBP2-type containing 1 (ZRANB1) is a positive modulator of Wnt signaling pathways. It hydrolyzes K29- and K33-linked ubiquitin chains.
특징 및 장점
Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.
물리적 형태
Supplied at 0.5 mg/mL in Tris saline with 0.02% sodium azide and 0.5% bovine serum albumin.
면책조항
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
An ankyrin-repeat ubiquitin-binding domain determines TRABID's specificity for atypical ubiquitin chains.
Licchesi JD
Nature Structural and Molecular Biology (2011)
K29-selective ubiquitin binding domain reveals structural basis of specificity and heterotypic nature of k29 polyubiquitin.
Kristariyanto YA
Molecular Cell (2015)
Rare copy number variation in cerebral palsy
Gai McMichael
European Journal of Human Genetics (2014)
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