FAM82A1 抗体 (AA 261-360) (Biotin)
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- 抗原 See all FAM82A1 (RMDN2) products
- FAM82A1 (RMDN2) (Regulator of Microtubule Dynamics 2 (RMDN2))
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抗原表位
- AA 261-360
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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 FAM82A1 antibody is conjugated to Biotin
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应用范围
- ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- Human,Mouse,Rat,Dog,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FAM82A1
- 亚型
- IgG
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anti-Regulator of Microtubule Dynamics 2 (RMDN2) antibody
RMDN2 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Regulator of Microtubule Dynamics 2 (RMDN2) (AA 396-445) antibodyRMDN2 适用: 人, 小鼠, Pig, 兔, Cow, 马 WB 宿主: 兔 Polyclonal unconjugated
anti-Regulator of Microtubule Dynamics 2 (RMDN2) (AA 432-481) antibodyRMDN2 适用: 人, 小鼠, 大鼠, Pig, 兔, Cow, 马, 犬, 猴 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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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
- FAM82A1 (RMDN2) (Regulator of Microtubule Dynamics 2 (RMDN2))
- 别名
- FAM82A1 (RMDN2 产品)
- 别名
- FAM82A antibody, FAM82A1 antibody, PRO34163 antibody, PYST9371 antibody, RMD-2 antibody, RMD2 antibody, RMD4 antibody, regulator of microtubule dynamics 2 antibody, RMDN2 antibody
- 背景
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Synonyms: BLOCK18, FAM82A, Fam82a1, Family with sequence similarity 82 member A, Family with sequence similarity 82, member A1, hRMD 2, hRMD 4, hRMD-2, hRMD4, MGC33318, Microtubule associated protein, Protein FAM82A1, Regulator of microtubule dynamics, Regulator of microtubule dynamics protein 2, RMD 2, RMD-2, RMD2, RMD2_HUMAN.
Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The FAM82A gene product has been provisionally designated FAM82A pending further characterization.
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