TTC8 抗体 (AA 251-330) (Cy3)
Quick Overview for TTC8 抗体 (AA 251-330) (Cy3) (ABIN1409583)
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 251-330
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交叉反应
- 人, 小鼠, 大鼠
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预测反应
- Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human BBS8
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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) (AA 71-120) antibodyTTC8 适用: 人, 马, 兔, Hamster, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Tetratricopeptide Repeat Domain 8 (TTC8) (Internal Region) antibodyVerified TTC8 适用: 人 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
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应用备注
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FCM 1:20-100
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- TTC8 (Tetratricopeptide Repeat Domain 8 (TTC8))
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别名
- BBS8/TTC8
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背景
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Synonyms: Bardet Biedl syndrome 8 protein, Bardet Biedl syndrome type 8, Bardet-Biedl syndrome 8 protein, BBS8, Tetratricopeptide repeat domain 8, Tetratricopeptide repeat protein 8, TPR repeat protein 8, TTC 8, Ttc8, TTC8_HUMAN.
Background: Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. BBS patients also have an increased risk of developing diabetes, hypertension, and congenital heart defects. BBS is a heterogeneous disorder mapping to eight genetic loci and encoding eight proteins, BBS1-BBS8. Five BBS proteins encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS2 contains two overlapping genes: BBS2L1 and BBS2L2. BBSL1 was re-named BBS7, whereas BBS2L2 independently funcitons as BBS1. BBS7 contains 672 amino acids and is expressed at low to moderate levels in most human tissues.
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途径
- Hedgehog Signaling
抗原
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