FAM98A 抗体 (AA 251-350) (Biotin)
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- 抗原 See all FAM98A 抗体
- FAM98A (Family with Sequence Similarity 98, Member A (FAM98A))
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抗原表位
- AA 251-350
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适用
- 人, 小鼠
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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 FAM98A 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))
- 交叉反应
- 人, 小鼠
- 预测反应
- Rat,Cow,Sheep,Pig,Horse,Chicken
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FAM98A
- 亚型
- IgG
- Top Product
- Discover our top product FAM98A Primary Antibody
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anti-Family with Sequence Similarity 98, Member A (FAM98A) (AA 1-220) antibody
FAM98A 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 98, Member A (FAM98A) antibodyFAM98A 适用: 人, 小鼠, 大鼠 IHC 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 98, Member A (FAM98A) (AA 1-518) antibodyFAM98A 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Family with Sequence Similarity 98, Member A (FAM98A) (AA 323-372) antibodyFAM98A 适用: 人, 小鼠, 大鼠, 兔, Cow, 犬, 马, Pig, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 98, Member A (FAM98A) (AA 432-481) antibodyFAM98A 适用: 人, 小鼠, 大鼠, 兔, Cow, 犬, 马, 豚鼠, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 98, Member A (FAM98A) (Middle Region) antibodyFAM98A 适用: 人, 小鼠, 大鼠, 兔, Cow, 犬, 马, 豚鼠 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
- FAM98A (Family with Sequence Similarity 98, Member A (FAM98A))
- 别名
- FAM98A (FAM98A 产品)
- 背景
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Synonyms: FAM 98A, Family with sequence similarity 98 member A, Hypothetical protein LOC25940, LOC25940, Protein FAM98A, FA98A_HUMAN.
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 FAM98 gene product has been provisionally designated FAM98 pending further characterization.
- 基因ID
- 25940
- 途径
- SARS-CoV-2 Protein Interactome
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