TTC8 抗体 (AA 271-533)
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Quick Overview for TTC8 抗体 (AA 271-533) (ABIN7873159)
抗原
See all TTC8 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 271-533
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原理
- BBS8 Antibody / Bardet-Biedl syndrome 8 / TTC8
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纯化方法
- Antigen affinity purified
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免疫原
- Recombinant human protein (amino acids E271-Q533) was used as the immunogen for the BBS8 antibody.
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亚型
- IgG
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anti-Tetratricopeptide Repeat Domain 8 (TTC8) (AA 416-514) antibody
TTC8 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 7E2 unconjugated
anti-Tetratricopeptide Repeat Domain 8 (TTC8) (AA 1-505) antibodyTTC8 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Tetratricopeptide Repeat Domain 8 (TTC8) (AA 251-330) antibodyTTC8 适用: 人, 小鼠, 大鼠 WB, ELISA, FACS, IF (cc), IF (p), IHC (fro), IHC (p), ICC 宿主: 兔 Polyclonal unconjugated
anti-Tetratricopeptide Repeat Domain 8 (TTC8) (AA 1-505) antibodyTTC8 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Tetratricopeptide Repeat Domain 8 (TTC8) (Internal Region) antibodyVerified TTC8 适用: 人 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Tetratricopeptide Repeat Domain 8 (TTC8) (AA 71-120) antibodyTTC8 适用: 人, 马, 兔, Hamster, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Tetratricopeptide Repeat Domain 8 (TTC8) (AA 18-46), (N-Term) antibodyTTC8 适用: 人 WB 宿主: 兔 Polyclonal RB36550 unconjugated
anti-Tetratricopeptide Repeat Domain 8 (TTC8) (AA 271-533) antibodyTTC8 适用: 人, 小鼠, 大鼠 WB, ELISA, FACS 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the BBS8 antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the BBS8 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- TTC8 (Tetratricopeptide Repeat Domain 8 (TTC8))
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别名
- BBS8
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背景
- Tetratricopeptide repeat domain 8 (TTC8) also known as Bardet-Biedl syndrome 8 (BBS8) is a protein that in humans is encoded by the TTC8 gene. This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is involved in the formation of cilia. A mutation in this gene has also been implicated in nonsyndromic retinitis pigmentosa. Alternative splicing results in multiple transcript variants.
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UniProt
- Q8TAM2
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途径
- Hedgehog Signaling
抗原
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