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- 抗原 See all OFD1 抗体
- OFD1 (Oral-Facial-Digital Syndrome 1 (OFD1))
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抗原表位
- Center
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This OFD1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 产品特性
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Rabbit Polyclonal antibody to OFD1 (oral-facial-digital syndrome 1)
OFD1 antibody - 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Recombinant protein encompassing a sequence within the center region of human OFD1. The exact sequence is proprietary.
- 亚型
- IgG
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- 应用备注
- Suggested dilution Reference IHC (Formalin-fixed paraffin-embedded sections) 1:100-1:1000* Western blot 1:1000-1:10000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceIHC (Formalin-fixed paraffin-embedded sections)1:100-1:1000* Western blot1:1000-1:10000*
- 说明
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Positive Control: Molt-4
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.96 mg/mL
- 缓冲液
- 0.1M Tris, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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Distinct Roles of TRAPPC8 and TRAPPC12 in Ciliogenesis via Their Interactions With OFD1." in: Frontiers in cell and developmental biology, Vol. 8, pp. 148, (2020) (PubMed).
: "
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Distinct Roles of TRAPPC8 and TRAPPC12 in Ciliogenesis via Their Interactions With OFD1." in: Frontiers in cell and developmental biology, Vol. 8, pp. 148, (2020) (PubMed).
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- 抗原
- OFD1 (Oral-Facial-Digital Syndrome 1 (OFD1))
- 别名
- OFD1 (OFD1 产品)
- 别名
- 71-7A antibody, CXorf5 antibody, JBTS10 antibody, RP23 antibody, SGBS2 antibody, RGD1562231 antibody, OFD1, centriole and centriolar satellite protein antibody, OFD1 antibody, ofd1 antibody, Ofd1 antibody
- 背景
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This gene is located on the X chromosome and encodes a centrosomal protein. A knockout mouse model has been used to study the effect of mutations in this gene. The mouse gene is also located on the X chromosome, however, unlike the human gene it is not subject to X inactivation. Mutations in this gene are associated with oral-facial-digital syndrome type I and Simpson-Golabi-Behmel syndrome type 2. Many pseudogenes have been identified, a single pseudogene is found on chromosome 5 while as many as fifteen have been found on the Y chromosome. Alternatively spliced transcripts have been described for this gene but the biological validity of these transcripts has not been determined.
Cellular Localization: Cytoplasm , Centrosome - 分子量
- 117 kDa
- 基因ID
- 8481
- 途径
- M Phase
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