PTCHD3 抗体 (AA 151-250) (AbBy Fluor® 680)
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- 抗原 See all PTCHD3 抗体
- PTCHD3 (Patched Domain Containing 3 (PTCHD3))
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抗原表位
- AA 151-250
- 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 PTCHD3 antibody is conjugated to AbBy Fluor® 680
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human PTCHD3
- 亚型
- IgG
- Top Product
- Discover our top product PTCHD3 Primary Antibody
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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
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- PTCHD3 (Patched Domain Containing 3 (PTCHD3))
- 别名
- PTCHD3 (PTCHD3 产品)
- 别名
- PTR antibody, 4930451E13Rik antibody, 4933440L20Rik antibody, RNDEu-3 antibody, patched domain containing 3 antibody, PTCHD3 antibody, Ptchd3 antibody
- 背景
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Synonyms: Patched domain containing 3, Patched domain-containing protein 3, Patched-related protein, Ptchd3, PTHD3_HUMAN, PTR.
Background: PTCHD3 is a 767 amino acid multi-pass membrane protein that localizes to the midpiece of the sperm tail, where it is implicated in sperm function and development. A member of the patched family, PTCHD3 contains one SSD (sterol-sensing) domain and is encoded by a gene that maps to human chromosome 10p12.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
- 基因ID
- 374308
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