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BCAP31 抗体
BCAP31
适用: 人, 小鼠, 大鼠
IF
宿主: 兔
Polyclonal
unconjugated
BCAP31抗体详情
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抗原
See all BCAP31 抗体
BCAP31
(B-Cell Receptor-Associated Protein 31 (BCAP31))
适用
All reactivities for BCAP31 抗体
人, 小鼠, 大鼠
宿主
All hosts for BCAP31 抗体
兔
克隆类型
All clonalities for BCAP31 抗体
多克隆
标记
All conjugates for BCAP31 抗体
This BCAP31 antibody is un-conjugated
应用范围
All applications for BCAP31 抗体
Immunofluorescence (IF)
产品特性
Polyclonal Antibody
纯化方法
Affinity purification
免疫原
Recombinant fusion protein of human BCAP31 (NP_001243376.1).
亚型
IgG
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Discover our top product BCAP31 Primary Antibody
Alternatives
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使用细节
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应用备注
IF 1:50-1:100
限制
仅限研究用
贮存及处理
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状态
Liquid
浓度
1 mg/mL
缓冲液
PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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
Store at -20°C. Avoid freeze / thaw cycles.
BCAP31目标详情
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抗原
BCAP31
(B-Cell Receptor-Associated Protein 31 (BCAP31))
别名
BCAP31 (BCAP31 产品 )
别名
6c6-ag antibody, bap31 antibody, cdm antibody, dxs1357e antibody, BCAP31 antibody, Bap31 antibody, 6C6-AG antibody, BAP31 antibody, CDM antibody, DXS1357E antibody, CALD1 antibody, caldesmon antibody, si:bz30i22.4 antibody, si:rp71-30i22.4 antibody, zgc:56389 antibody, B-cell receptor associated protein 31 antibody, receptor-associated protein antibody, lipopeptide mating pheromone precursor bap3-1 antibody, B cell receptor associated protein 31 antibody, B-cell receptor-associated protein 31 antibody, B-cell receptor associated protein 31 L homeolog antibody, bcap31 antibody, BAP31 antibody, bap3-1 antibody, BCAP31 antibody, Bcap31 antibody, bcap31.L antibody
背景
This gene encodes a member of the B-cell receptor associated protein 31 superfamily. The encoded protein is a multi-pass transmembrane protein of the endoplasmic reticulum that is involved in the anterograde transport of membrane proteins from the endoplasmic reticulum to the Golgi and in caspase 8-mediated apoptosis. Microdeletions in this gene are associated with contiguous ABCD1/DXS1375E deletion syndrome (CADDS), a neonatal disorder. Alternative splicing of this gene results in multiple transcript variants. Two related pseudogenes have been identified on chromosome 16.
基因ID
10134
UniProt
P51572
途径
Positive Regulation of Endopeptidase Activity
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