NIPAL2 抗体 (AA 1-100) (Biotin)
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- 抗原 See all NIPAL2 products
- NIPAL2 (NIPA-Like Domain Containing 2 (NIPAL2))
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抗原表位
- AA 1-100
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适用
- 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 NIPAL2 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Cow,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human NIPAL2
- 亚型
- IgG
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anti-NIPA-Like Domain Containing 2 (NIPAL2) (N-Term) antibody
NIPAL2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-NIPA-Like Domain Containing 2 (NIPAL2) (AA 57-86), (N-Term) antibodyNIPAL2 适用: 小鼠, 人 WB 宿主: 兔 Polyclonal RB26693 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
- NIPAL2 (NIPA-Like Domain Containing 2 (NIPAL2))
- 别名
- NIPAL2 (NIPAL2 产品)
- 别名
- NPAL2 antibody, 9330161F08Rik antibody, Npal2 antibody, RGD1564315 antibody, NIPA like domain containing 2 antibody, NIPA-like domain containing 2 antibody, NIPAL2 antibody, Nipal2 antibody
- 背景
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Synonyms: NIPA like domain containing 2, NIPAL2, NPAL2, NPAL2_HUMAN.
Background: Non-imprinted in Prader-Willi/Angelman syndrome (NIPA) proteins are highly conserved receptors or transporters. A family known as the NIPA-like domain containing (NPAL) proteins are closely related to the NIPA proteins, but most are uncharacterized and their functions are unknown. NPAL2 (NIPA-like domain containing 2), also known as NIPAL2, is a 368 amino acid multi-pass membrane protein belonging to the NIPA family and is encoded by a gene located on human chromosome 8. Human chromosome 8 consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.
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