NIR1 抗体 (AA 131-250)
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- 抗原 See all NIR1 (PITPNM3) 抗体
- NIR1 (PITPNM3) (PITPNM Family Member 3 (PITPNM3))
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抗原表位
- AA 131-250
- 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 NIR1 antibody is un-conjugated
- 应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Cow,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human NIR1/RDGBA3
- 亚型
- IgG
- Top Product
- Discover our top product PITPNM3 Primary Antibody
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- 应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- NIR1 (PITPNM3) (PITPNM Family Member 3 (PITPNM3))
- 别名
- NIR1 (PITPNM3 产品)
- 别名
- ACKR6 antibody, CORD5 antibody, NIR1 antibody, RDGBA3 antibody, A330068P14Rik antibody, AI848332 antibody, Ackr6 antibody, Gm880 antibody, PITPNM family member 3 antibody, PITPNM3 antibody, Pitpnm3 antibody
- 背景
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Synonyms: membrane-associated 3, CORD5, Membrane associated phosphatidylinositol transfer protein 3, Membrane-associated phosphatidylinositol transfer protein 3, NIR 1, NIR-1, NIR1, Phosphatidylinositol transfer protein, Phosphatidylinositol transfer protein, membrane-associated 3, PITM3_HUMAN, PITPnm 3, PITPNM, PITPNM family member 3, Pitpnm3, PYK2 N terminal domain interacting receptor 1, PYK2 N-terminal domain-interacting receptor 1, RDGBA3, retinal degeneration B alpha 3.
Background: Catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes (in vitro) (By similarity). Binds calcium ions.Involvement in disease:Defects in PITPNM3 are the cause of cone-rod dystrophy type 5 (CORD5) . CORDs are inherited retinal dystrophies belonging to the group of pigmentary retinopathies. CORDs are characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration.
- 基因ID
- 83394
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