PDZD7 抗体 (AbBy Fluor® 555)
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- 抗原 See all PDZD7 抗体
- PDZD7 (PDZ Domain Containing 7 (PDZD7))
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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 PDZD7 antibody is conjugated to AbBy Fluor® 555
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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 PDZD7
- 亚型
- IgG
- Top Product
- Discover our top product PDZD7 Primary Antibody
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anti-PDZ Domain Containing 7 (PDZD7) (AA 1-511) antibody
PDZD7 适用: 人 WB 宿主: 小鼠 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
- PDZD7 (PDZ Domain Containing 7 (PDZD7))
- 别名
- PDZD7 (PDZD7 产品)
- 别名
- PDZK7 antibody, Pdzk7 antibody, PDZD7 antibody, DKFZp459K1926 antibody, si:dkey-158p2.1 antibody, 9130207N01 antibody, EG435601 antibody, PDZ domain containing 7 antibody, PDZ domain containing 7a antibody, PDZD7 antibody, Pdzd7 antibody, pdzd7a antibody
- 背景
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Synonyms: PDZ domain containing 7, PDZK7, RP11-108L7.9, EG435601, OTTMUSP00000044305, 9130207N01, OTTMUSP00000044304, PDZD7_HUMAN.
Background: PDZK7, also known as PDZD7, is a 517 amino acid protein that contains two PDZ (DHR) domains. Encoded by a gene that maps to human chromosome 10q24.31, PDZK7 is conserved in dog, mouse and rat, and exists as three alternatively spliced isoforms. PDZK7 is known to interact with Harmonin, MASS1, USH1G and Usherin. Localizing to nucleus, PDZK7 is expressed in retinal pigment epithelium and inner ear. Biallelic inactivation of PDZK7 can cause non-syndromic hearing impairment and chromosomal aberrations, which are linked to non-syndromic sensorineural deafness. PDZK7 mutations are also linked to Usher syndrome, which is characterized by retinitis pigmentosa and sensorineural deafness, and Alzheimer disease. The gene that encodes PDZK7 maps to human chromosome 10q24.31.
- 基因ID
- 79955
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