LRRC41 抗体 (AA 331-430) (Cy3)
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- 抗原 See all LRRC41 抗体
- LRRC41 (Leucine Rich Repeat Containing 41 (LRRC41))
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抗原表位
- AA 331-430
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适用
- 人, 大鼠, 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 LRRC41 antibody is conjugated to Cy3
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 预测反应
- Dog,Cow,Sheep,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human LRRC41
- 亚型
- IgG
- Top Product
- Discover our top product LRRC41 Primary Antibody
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anti-Leucine Rich Repeat Containing 41 (LRRC41) (AA 86-195) antibody
LRRC41 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Leucine Rich Repeat Containing 41 (LRRC41) (Internal Region) antibodyLRRC41 适用: 人, 大鼠, 小鼠 WB, ELISA, IHC, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Leucine Rich Repeat Containing 41 (LRRC41) antibodyLRRC41 适用: 人, 大鼠, 小鼠, Cow WB, IHC 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
- LRRC41 (Leucine Rich Repeat Containing 41 (LRRC41))
- 别名
- LRRC41 (LRRC41 产品)
- 别名
- LRRC41 antibody, MUF1 antibody, RP4-636H5.2 antibody, AA409966 antibody, AW555107 antibody, D630045E04Rik antibody, D730026A16Rik antibody, RGD1311221 antibody, MGC137526 antibody, leucine rich repeat containing 41 antibody, leucine-rich repeat-containing protein 41 antibody, LRRC41 antibody, lrrc41 antibody, LOC100550348 antibody, Lrrc41 antibody
- 背景
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Synonyms: elongin BC interacting leucine rich repeat protein, Leucine rich repeat containing 41, Leucine rich repeat containing protein 41, MUF1, PP7759, LRC41_HUMAN.
Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
- 基因ID
- 10489
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