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- 抗原 See all FAM76B products
- FAM76B (Family with Sequence Similarity 76, Member B (FAM76B))
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适用
- 人, 小鼠, 大鼠
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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 FAM76B antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FAM76B
- 亚型
- IgG
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anti-Family with Sequence Similarity 76, Member B (FAM76B) (AA 108-157) antibody
FAM76B 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 小鸡, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 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
- FAM76B (Family with Sequence Similarity 76, Member B (FAM76B))
- 别名
- FAM76B (FAM76B 产品)
- 别名
- fa11h02 antibody, wu:fa11h02 antibody, zgc:73333 antibody, 2810485I05Rik antibody, C78303 antibody, RGD1311077 antibody, family with sequence similarity 76 member B antibody, family with sequence similarity 76, member B antibody, family with sequence similarity 76 member B S homeolog antibody, FAM76B antibody, fam76b antibody, fam76b.S antibody, Fam76b antibody
- 背景
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Synonyms: Family with sequence similarity 76 member B, Hypothetical protein LOC143684, MGC33371, FA76B_HUMAN.
Background: With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 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. 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. The FAM76B gene product has been provisionally designated FAM76B pending further characterization.
- 基因ID
- 143684
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