FAM81A 抗体 (AA 281-368) (FITC)
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- 抗原 See all FAM81A products
- FAM81A (Family with Sequence Similarity 81, Member A (FAM81A))
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抗原表位
- AA 281-368
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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 FAM81A antibody is conjugated to FITC
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应用范围
- Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- 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 FAM81A
- 亚型
- IgG
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anti-Family with Sequence Similarity 81, Member A (FAM81A) (AA 143-192) antibody
FAM81A 适用: 人, 大鼠, Cow, 犬, 马, Pig, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 81, Member A (FAM81A) (AA 71-120) antibodyFAM81A 适用: 人, 大鼠, 小鼠, Cow, 犬, 马, 兔, 豚鼠, Pig, 猴, Bat WB 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 81, Member A (FAM81A) (N-Term) antibodyFAM81A 适用: 人, 大鼠, 小鼠, Cow, 犬, 马, 兔, 豚鼠 WB 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
- FAM81A (Family with Sequence Similarity 81, Member A (FAM81A))
- 别名
- FAM81A (FAM81A 产品)
- 别名
- 6430514L14Rik antibody, RGD1311958 antibody, family with sequence similarity 81, member A antibody, family with sequence similarity 81 member A antibody, Fam81a antibody, FAM81A antibody
- 背景
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Synonyms: FA81B_HUMAN, FAM81B, Family with sequence similarity 81, member B, FLJ25333, Hypothetical protein LOC153643, Protein FAM81B.
Background: Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.
- 基因ID
- 145773
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