BRP44 抗体 (AA 21-100) (Biotin)
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- 抗原 See all BRP44 抗体
- BRP44 (Brain Protein 44 (BRP44))
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抗原表位
- AA 21-100
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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 BRP44 antibody is conjugated to Biotin
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应用范围
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 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 BRP44
- 亚型
- IgG
- Top Product
- Discover our top product BRP44 Primary Antibody
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anti-Brain Protein 44 (BRP44) (AA 1-40) antibody
BRP44 适用: 人 ELISA, WB, IHC 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
- BRP44 (Brain Protein 44 (BRP44))
- 别名
- BRP44 (BRP44 产品)
- 别名
- BRP44 antibody, 0610006C01Rik antibody, 2010002I07Rik antibody, 2610205H19Rik antibody, AA108335 antibody, Brp44 antibody, ESTM43 antibody, brp44 antibody, wu:fb22b02 antibody, wu:fb22g07 antibody, zgc:56391 antibody, zgc:86614 antibody, MGC53394 antibody, DKFZp459F1815 antibody, RGD1563422 antibody, mitochondrial pyruvate carrier 2 antibody, mitochondrial pyruvate carrier 2 S homeolog antibody, uncharacterized protein antibody, MPC2 antibody, Mpc2 antibody, mpc2 antibody, mpc2.S antibody, LOC706595 antibody, LOC100285678 antibody
- 背景
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Synonyms: ESTM43, MGC125753, BR44_HUMAN, Brain protein 44, BRP44, DKFZp564B167, MGC125752, rCG_46381, RGD1563422, RP1-295C6.1.
Background: BRP44 is a 127 amino acid protein belonging to the UPF0041 family. The gene that encodes BRP44 maps to human chromosome 1, which 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
- 25874
- 途径
- Warburg Effect
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