FAM168A 抗体 (AA 75-180) (Biotin)
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- 抗原 See all FAM168A products
- FAM168A (Family with Sequence Similarity 168, Member A (FAM168A))
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抗原表位
- AA 75-180
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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 FAM168A antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Cow,Sheep,Pig
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FAM168A/TCRP1
- 亚型
- IgG
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anti-Family with Sequence Similarity 168, Member A (FAM168A) (AA 44-93) antibody
FAM168A 适用: 人, 小鼠, Cow, 犬, 豚鼠, 马, 兔, 大鼠, Bat, 小鸡, 猴, Pig, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 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 for 12 months.
- 有效期
- 12 months
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- 抗原
- FAM168A (Family with Sequence Similarity 168, Member A (FAM168A))
- 别名
- TCRP1 (FAM168A 产品)
- 别名
- KIAA0280 antibody, TCRP1 antibody, 2610030B18Rik antibody, B930006L02Rik antibody, mKIAA0280 antibody, family with sequence similarity 168 member A antibody, family with sequence similarity 168, member A antibody, FAM168A antibody, Fam168a antibody
- 背景
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Synonyms: F168A_HUMAN, Fam168a, KIAA0280, Protein FAM168A, TCRP1, Tongue cancer chemotherapy resistance-associated protein 1.
Background: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
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