FIBIN 抗体 (AA 101-200) (Biotin)
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- 抗原 See all FIBIN 抗体
- FIBIN (Fin Bud Initiation Factor Homolog (FIBIN))
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抗原表位
- AA 101-200
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适用
- 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 FIBIN antibody is conjugated to Biotin
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应用范围
- ELISA, Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Cow,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FIBIN
- 亚型
- IgG
- Top Product
- Discover our top product FIBIN Primary Antibody
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anti-Fin Bud Initiation Factor Homolog (FIBIN) (AA 101-200) antibody
FIBIN 适用: 小鼠 ELISA, WB, IF (p), IF (cc), IHC (fro), IHC (p), ICC 宿主: 兔 Polyclonal unconjugated
anti-Fin Bud Initiation Factor Homolog (FIBIN) (AA 1-211) antibodyFIBIN 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
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
- FIBIN (Fin Bud Initiation Factor Homolog (FIBIN))
- 别名
- FIBIN (FIBIN 产品)
- 别名
- 1110018M03Rik antibody, fibin antibody, sb:cb374 antibody, zgc:110676 antibody, fin bud initiation factor homolog (zebrafish) antibody, fin bud initiation factor b antibody, FIBIN antibody, Fibin antibody, fibinb antibody
- 背景
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Synonyms: Fin bud initiation factor homolog, FIBIN, PSEC0235
Background: FIBIN (Fin bud initiation factor homolog) is a 211 amino acid protein involved in fin initiation in zebrafish. The human homolog is encoded by a gene that maps to chromosome 11, which 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.
- 基因ID
- 387758
- UniProt
- Q8TAL6
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