ODF3B 抗体 (Alexa Fluor 488)
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- 抗原 See all ODF3B products
- ODF3B (Outer Dense Fiber of Sperm Tails 3B (ODF3B))
- 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 ODF3B antibody is conjugated to Alexa Fluor 488
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (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 ODF3B
- 亚型
- IgG
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anti-Outer Dense Fiber of Sperm Tails 3B (ODF3B) (AA 19-47), (N-Term) antibody
ODF3B 适用: 人, 小鼠 WB, IHC (p) 宿主: 兔 Polyclonal RB28703 unconjugated
anti-Outer Dense Fiber of Sperm Tails 3B (ODF3B) (AA 22-51), (N-Term) antibodyODF3B 适用: 人, 小鼠 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- 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
- 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
- ODF3B (Outer Dense Fiber of Sperm Tails 3B (ODF3B))
- 别名
- ODF3B (ODF3B 产品)
- 别名
- ODF3L3 antibody, 2010001J22Rik antibody, RGD1564322 antibody, fj19d04 antibody, odf3l antibody, si:dkeyp-1h4.4 antibody, wu:fj19d04 antibody, zgc:63985 antibody, outer dense fiber of sperm tails 3B antibody, ODF3B antibody, Odf3b antibody, odf3b antibody
- 背景
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Synonyms: ODF3B, ODF3B_HUMAN, Odf3l3, Outer dense fiber of sperm tails 3B, Outer dense fiber protein 3-like protein 3, Outer dense fiber protein 3B.
Background: ODF3B, also known as ODF3L3 (outer dense fiber protein 3-like protein 3), is a 253 amino acid protein belonging to the ODF3 family. Existing as two isoforms produced by alternative splicing, ODF3B contains one DUF1309 repeat. The gene that encodes ODF3B maps to human chromosome 22, which contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
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