TDRP/C8orf42 抗体 (AA 51-150) (FITC)
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- 抗原 See all TDRP/C8orf42 (TDRP) 抗体
- TDRP/C8orf42 (TDRP) (Testis Development Related Protein (TDRP))
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抗原表位
- AA 51-150
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适用
- 大鼠
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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 TDRP/C8orf42 antibody is conjugated to FITC
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 大鼠
- 预测反应
- Human,Mouse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C8orf42
- 亚型
- IgG
- Top Product
- Discover our top product TDRP Primary Antibody
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anti-Testis Development Related Protein (TDRP) (AA 51-150) antibody
TDRP 适用: 大鼠 WB, IF (cc), IF (p), IHC (fro), IHC (p), ELISA, ICC 宿主: 兔 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
- 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
- TDRP/C8orf42 (TDRP) (Testis Development Related Protein (TDRP))
- 别名
- C8orf42 (TDRP 产品)
- 别名
- C8orf42 antibody, Inm01 antibody, TDRP1 antibody, TDRP2 antibody, 2610019F03Rik antibody, c8orf42 antibody, testis development related protein antibody, testis development related protein L homeolog antibody, TDRP antibody, Tdrp antibody, tdrp.L antibody
- 背景
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Synonyms: C8orf42, TDRP_HUMAN, Protein INM01, Protein TDRP, Uncharacterized protein C8orf42.
Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf42 gene product has been provisionally designated C8orf42 pending further characterization.
- 基因ID
- 157695
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