ANKRD20A1 抗体
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- 抗原 See all ANKRD20A1 products
- ANKRD20A1 (Ankyrin Repeat Domain 20 Family, Member A1 (ANKRD20A1))
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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 ANKRD20A1 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
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ANKRD20A1
- 亚型
- IgG
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anti-Ankyrin Repeat Domain 20 Family, Member A1 (ANKRD20A1) antibody
ANKRD20A1 适用: 人, 小鼠 WB, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Ankyrin Repeat Domain 20 Family, Member A1 (ANKRD20A1) (AA 1-823) antibodyANKRD20A1 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
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
- ANKRD20A1 (Ankyrin Repeat Domain 20 Family, Member A1 (ANKRD20A1))
- 别名
- ANKRD20A1 (ANKRD20A1 产品)
- 别名
- ANKRD20A antibody, ankyrin repeat domain 20 family member A1 antibody, ANKRD20A1 antibody
- 背景
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Synonyms: A20A1_HUMAN, ANKRD20A, ANKRD20A1, Ankyrin repeat domain 20 family member A1, Ankyrin repeat domain 20A, Ankyrin repeat domain containing protein 20A1, Ankyrin repeat domain-containing protein 20A1, DKFZp434A171.
Background: Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD20A (ankyrin repeat domain-containing protein 20A) is an 823 amino acid protein that contains five ANK repeats. The gene encoding ANKRD20A maps to chromosome 9, which consists of about 145 million bases and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and familial dysautonomia are associated with chromosome 9. Also, chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
- 基因ID
- 84210
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