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C16orf57 抗体 (N-Term)
USB1
适用: 人
WB
宿主: 兔
Polyclonal
unconjugated
C16orf57抗体详情
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抗原
See all C16orf57 (USB1) 抗体
C16orf57 (USB1)
(U6 SnRNA Biogenesis 1 (USB1))
抗原表位
All epitopes for C16orf57 抗体
N-Term
适用
All reactivities for C16orf57 抗体
人
宿主
All hosts for C16orf57 抗体
兔
克隆类型
All clonalities for C16orf57 抗体
多克隆
标记
All conjugates for C16orf57 抗体
This C16orf57 antibody is un-conjugated
应用范围
All applications for C16orf57 抗体
Western Blotting (WB)
序列
LVGYSSSGSE DESEDGMRTR PGDGSHRRGQ SPLPRQRFPV PDSVLNMFPG
纯化方法
Affinity purified
免疫原
The immunogen is a synthetic peptide directed towards the N terminal region of human C16ORF57
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Discover our top product USB1 Primary Antibody
Alternatives
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anti-U6 SnRNA Biogenesis 1 (USB1) (AA 150-199) antibody
USB1
适用: 人, 小鼠, 大鼠, 马, Pig, Cow, 兔, 犬, 豚鼠, 猴, Hamster
WB
宿主: 兔
Polyclonal
unconjugated
使用细节
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应用备注
Optimal working dilution should be determined by the investigator.
限制
仅限研究用
贮存及处理
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状态
Liquid
缓冲液
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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
-20 °C
储存方法
For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
C16orf57目标详情
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抗原
C16orf57 (USB1)
(U6 SnRNA Biogenesis 1 (USB1))
别名
C16ORF57 (USB1 产品 )
别名
C16orf57 antibody, HVSL1 antibody, Mpn1 antibody, PN antibody, hUsb1 antibody, C18H16orf57 antibody, AA960436 antibody, RGD1305215 antibody, c16orf57 antibody, C2H16orf57 antibody, zgc:91896 antibody, U6 snRNA biogenesis phosphodiesterase 1 antibody, U6 snRNA biogenesis 1 antibody, U6 snRNA biogenesis phosphodiesterase 1 L homeolog antibody, USB1 antibody, Usb1 antibody, usb1.L antibody, usb1 antibody
背景
This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. Alias Symbols: PN, Mpn1, HVSL1, hUsb1, C16orf57 Protein Size: 186
基因ID
79650
NCBI登录号
NM_001195302 , NP_001182231
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