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CIRH1A 抗体 (N-Term)
CIRH1A
适用: 人
WB, FACS, IHC (p)
宿主: 兔
Polyclonal
RB23136
unconjugated
CIRH1A抗体详情
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抗原
See all CIRH1A 抗体
CIRH1A
(Cirrhosis, Autosomal Recessive 1A (Cirhin) (CIRH1A))
抗原表位
All epitopes for CIRH1A 抗体
AA 116-143, N-Term
适用
All reactivities for CIRH1A 抗体
人
宿主
All hosts for CIRH1A 抗体
兔
克隆类型
All clonalities for CIRH1A 抗体
多克隆
标记
All conjugates for CIRH1A 抗体
This CIRH1A antibody is un-conjugated
应用范围
All applications for CIRH1A 抗体
Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
纯化方法
This antibody is purified through a protein A column, followed by peptide affinity purification.
免疫原
This CIRH1A antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 116-143 amino acids from the N-terminal region of human CIRH1A.
克隆位点
RB23136
亚型
Ig Fraction
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Discover our top product CIRH1A Primary Antibody
Alternatives
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使用细节
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应用备注
WB: 1:1000. IHC-P: 1:50~100. FC: 1:10~50
限制
仅限研究用
贮存及处理
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状态
Liquid
缓冲液
Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
储存液
Sodium azide
注意事项
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
储存条件
4 °C,-20 °C
储存方法
Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
有效期
6 months
CIRH1A目标详情
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抗原
CIRH1A
(Cirrhosis, Autosomal Recessive 1A (Cirhin) (CIRH1A))
别名
CIRH1A (CIRH1A 产品 )
别名
cirhin antibody, Cirhin antibody, Naic antibody, Teg-292 antibody, Tex292 antibody, naic antibody, tex292 antibody, zgc:77199 antibody, wu:fi09g10 antibody, wu:fi37c02 antibody, CIRH1A antibody, CIRHIN antibody, NAIC antibody, TEX292 antibody, UTP4 antibody, UTP4, small subunit processome component antibody, UTP4 small subunit processome component antibody, UTP4 small subunit processome component L homeolog antibody, UTP4 antibody, Utp4 antibody, utp4 antibody, utp4.L antibody
背景
CIRH1A encodes a WD40-repeat-containing protein that is localized to the nucleolus. Mutation of this gene causes North American Indian childhood cirrhosis, a severe intrahepatic cholestasis that results in transient neonatal jaundice, and progresses to periportal fibrosis and cirrhosis in childhood and adolescence.
分子量
76890
基因ID
84916
NCBI登录号
NP_116219
UniProt
Q969X6
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