FAM89B 抗体 (AA 41-150) (Alexa Fluor 555)
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- 抗原 See all FAM89B products
- FAM89B (Family with Sequence Similarity 89, Member B (FAM89B))
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抗原表位
- AA 41-150
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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 FAM89B antibody is conjugated to Alexa Fluor 555
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FAM89B/MMTV-R
- 亚型
- IgG
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anti-Family with Sequence Similarity 89, Member B (FAM89B) antibody
FAM89B 适用: 人 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 89, Member B (FAM89B) (AA 1-162) antibodyFAM89B 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 89, Member B (FAM89B) antibodyFAM89B 适用: 小鼠, 兔 ELISA, WB 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
- FAM89B (Family with Sequence Similarity 89, Member B (FAM89B))
- 别名
- FAM89B (FAM89B 产品)
- 别名
- MTVR1 antibody, 1110021A21Rik antibody, MMTV antibody, Mtvr2 antibody, family with sequence similarity 89 member B antibody, family with sequence similarity 89, member B antibody, FAM89B antibody, Fam89b antibody
- 背景
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Synonyms: Family with sequence similarity 89 member B, Mammary tumor virus receptor 2v Mammary turmor virus receptor homolog 1, MMTVR, MMTVR2, MTVR1, Protein FAM89B, FA89B_HUMAN.
Background: Mtvr1 is a 176 amino acid protein that exists as two alternatively spliced isoforms. Belonging to the FAM89 family, Mtvr1 is encoded by a gene that maps to human chromosome 11, which comprises approximately 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11-encoded genes.
- 基因ID
- 23625
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