CCDC88B 抗体 (AA 1271-1476) (Cy5)
Quick Overview for CCDC88B 抗体 (AA 1271-1476) (Cy5) (ABIN888265)
抗原
See all CCDC88B 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 1271-1476
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预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human CCDC88B/BRLZ
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亚型
- IgG
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anti-Coiled-Coil Domain Containing 88B (CCDC88B) (AA 1-223) antibody
CCDC88B 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- CCDC88B (Coiled-Coil Domain Containing 88B (CCDC88B))
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别名
- CCDC88B
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背景
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Synonyms: Brain leucine zipper domain containing protein, Brain leucine zipper domain-containing protein, Brain leucine zipper protein, BRLZ, CC88B_HUMAN, CCDC 88, CCDC 88B, Ccdc88b, Coiled coil domain containing 88, Coiled coil domain containing protein 88B, Coiled-coil domain-containing protein 88B, DKFZp434G0920, FLJ00354, FLJ37970, HkRP 3, HkRP3, Hook related protein 3, Hook-related protein 3.
Background: HkRP3, also known as CCDC88B (coiled-coil domain-containing protein 88B) or BRLZ (brain leucine zipper domain-containing protein), is a 1,476 amino acid protein that belongs to the CCDC88 family. Members of the hook-related protein family are characterized by the presence of a C-terminal hook-related domain and an N-terminal potential microtubule binding domain. HkRP3 may be involved in the linkage of various organelles to microtubules, and exists as six alternatively spliced isoforms. The gene encoding HkRP3 maps to human chromosome 11q13.1 and mouse chromosome 19 A. Chromosome 11 houses over 1,400 genes and comprises nearly 4 % of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
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基因ID
- 283234
抗原
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