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Thermo Fisher Scientific UGT1A1 Recombinant Rabbit Monoclonal Antibody (8U9P3)
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Thermo Fisher Scientific UGT1A1 Recombinant Rabbit Monoclonal Antibody (8U9P3)

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UGT1A1 단백질을 인식하는 토끼 유래 재조합 단클론 항체. Western blot과 ELISA에 적합하며, 인간, 마우스, 랫트 반응성. 고순도 친화 크로마토그래피 정제, 액상 형태로 안정적 보관 가능.

카탈로그번호
MA551266
판매단위
pk
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마지막 업데이트 2025. 07. 26. 오전 02:46
Thermo Fisher Scientific MA551266 UGT1A1 Recombinant Rabbit Monoclonal Antibody (8U9P3) 100 ul pk판매 단위 pk ·
재고 확인 필요
658,900원VAT 포함 724,790원

Thermo Fisher Scientific · Thermo Fisher Scientific UGT1A1 Recombinant Rabbit Monoclonal Antibody (8U9P3)

Applications

Application Tested Dilution
Western Blot (WB) 1:2,000–1:4,000
ELISA 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone 8U9P3
Immunogen A synthetic peptide corresponding to a sequence within amino acids 101–200 of human UGT1A1 (NP_000454.1)
Conjugate Unconjugated
Form Liquid
Concentration 0.43 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.3, with 0.05% BSA, 50% glycerol
Contains 0.05% ProClin 300
Storage Conditions −20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_3094323

Product Specific Information

Immunogen sequence:
ENDSFLQRVI KTYKKIKKDS AMLLSGCSHL LHNKELMASL AESSFDVMLT DPFLPCSPIV AQYLSLPTVF FLHALPCSLE FEATQCPNPF SYVPRPLSSH

Target Information

This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites.
This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5′ exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini.
Each first exon encodes the substrate binding site and is regulated by its own promoter. The preferred substrate of this enzyme is bilirubin, although it also has moderate activity with simple phenols, flavones, and C18 steroids.
Mutations in this gene result in Crigler-Najjar syndromes types I and II and in Gilbert syndrome.


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

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