추천 제품
생물학적 소스
rabbit
Quality Level
결합
unconjugated
항체 형태
affinity isolated antibody
항체 생산 유형
primary antibodies
클론
polyclonal
양식
buffered aqueous solution
분자량
antigen ~70 kDa
종 반응성
mouse, human
농도
~1.0 mg/mL
기술
immunoprecipitation (IP): 5-10 μg using lysate of mouse brain
indirect immunofluorescence: suitable
western blot: 2-4 μg/mL using whole extract of HEK-293T cells expressing human HRD1/SYVN1.
UniProt 수납 번호
배송 상태
dry ice
저장 온도
−20°C
타겟 번역 후 변형
unmodified
유전자 정보
human ... SYVN1(84447)
mouse ... Syvn1(74126)
rat ... Syvn1(361712)
일반 설명
Synoviolin (SYVN1) is an endoplasmic reticulum (ER)-membrane resident E3 ubiquitin ligase. The SYVN1 gene is mapped to human chromosome 11q13.1. Also known as HRD1, this protein has five transmembrane domains and a really interesting new gene (RING) finger domain.
특이성
Anti-HRD1/SYVN1 recognizes human and mouse HRD1/SYVN1.
애플리케이션
Anti-HRD1/SYVN1 antibody produced in rabbit has been used in immunoblotting and immunoprecipitation.
생화학적/생리학적 작용
Synoviolin (SYVN1) protects against endoplasmic reticulum (ER) stress-induced apoptosis through ER stress-associated protein degradation (ERAD). The really interesting new gene (RING) finger domain of SYVN1 mediates the transfer of ubiquitin from E2 to substrates and a proline-rich domain. E3 ubiquitin-protein ligase (HRD1) expression is strongly induced by ER stress. HRD1 interacts with parkin-associated endothelin receptor-like receptor (Pael-R), promoting its degradation, and protects neurons from cell death caused by the accumulation of Pael-R. HRD1 is also found to enhance the degradation and suppress the toxicity of polyglutamine-expanded huntingtin. In addition to its role in ERAD, HRD1 targets tumor suppressor gene p53 for proteasomal degradation. Overexpression of HRD1 is implicated in the pathogenesis of rheumatoid arthritis. The deletion of gene locus of SYVN1 is implicated in spastic paraplegia, optic atrophy, and neuropathy (SPOAN) disorder.
물리적 형태
Solution in 0.01 M phosphate buffered saline pH 7.4, containing 15 mM sodium azide.
저장 및 안정성
For continuous use, store at 2–8 °C for up to one month. For extended storage, freeze in working aliquots at –20 °C. Repeated freezing and thawing is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.
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
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
가장 최신 버전 중 하나를 선택하세요:
Journal of neuroscience research, 86(7), 1577-1587 (2008-02-05)
HRD1 is an E3 ubiquitin ligase and plays an important role in endoplasmic reticulum-associated degradation (ERAD). Parkin-associated endothelin receptor-like receptor (Pael-R) is a substrate of the E3 ubiquitin ligase parkin, which has been implicated in ER stress-induced cell death in
PloS one, 10(3), e0119955-e0119955 (2015-03-26)
By suppressing neuronal apoptosis, Icariin is a potential therapeutic drug for neuronal degenerative diseases. The molecular mechanisms of Icariin anti-apoptotic functions are still largely unclear. In this report, we found that Icariin induces the expression of Synoviolin, an endoplasmic reticulum
Journal of cell science, 128(22), 4112-4125 (2015-10-09)
Clearance of misfolded proteins from the endoplasmic reticulum (ER) is mediated by the ubiquitin-proteasome system in a process known as ER-associated degradation (ERAD). The mechanisms through which proteins containing aberrant transmembrane domains are degraded by ERAD are poorly understood. To
iScience, 23(9), 101494-101494 (2020-09-12)
Atlastin (ATL) is a class of dynamin-like GTPases shaping endoplasmic reticulum (ER) by mediating homotypic membrane fusion. Defect of ATLs leads to abnormal ER structure and hereditary spastic paraplegia (HSP), a neurodegenerative disease with progressive spasticity. How ATLs are regulated
Nature communications, 8(1), 1472-1472 (2017-11-15)
Endoplasmic-reticulum-associated degradation (ERAD) is an important protein quality control system which maintains protein homeostasis. Constituents of the ERAD complex and its role in neurodegeneration are not yet fully understood. Here, using proteomic and FRET analyses, we demonstrate that the ER
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