BBS2 抗体 (N-Term)
Quick Overview for BBS2 抗体 (N-Term) (ABIN2788195)
抗原
See all BBS2 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- N-Term
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序列
- GSDLFWTVTG DNVNSLALCD FDGDGKKELL VGSEDFDIRV FKEDEIVAEM
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预测反应
- Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 93%, Rabbit: 100%, Rat: 100%, Zebrafish: 79%
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产品特性
- This is a rabbit polyclonal antibody against BBS2. It was validated on Western Blot.
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纯化方法
- Affinity Purified
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免疫原
- The immunogen is a synthetic peptide directed towards the N terminal region of human BBS2
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anti-Bardet-Biedl Syndrome 2 (BBS2) (AA 1-96) antibody
BBS2 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 2 (BBS2) (C-Term) antibodyBBS2 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 2 (BBS2) antibodyBBS2 适用: 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 2 (BBS2) (AA 1-721) antibodyBBS2 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 2 (BBS2) (AA 151-200) antibodyBBS2 适用: 人, 犬, Cow, 马, 兔, 斑马鱼, 豚鼠, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 2 (BBS2) (AA 315-364) antibodyBBS2 适用: 人, 小鼠, 犬, Cow, 马, 兔, 斑马鱼, Bat, 小鸡 WB 宿主: 兔 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 2 (BBS2) (N-Term) antibodyBBS2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal working dilutions should be determined experimentally by the investigator.
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说明
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Antigen size: 721 AA
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- Lot specific
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缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- Avoid repeated freeze-thaw cycles.
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储存条件
- -20 °C
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储存方法
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
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别名
- BBS2
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背景
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This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene forms a multiprotein BBSome complex with six other BBS proteins.
Alias Symbols: BBS, MGC20703
Protein Interaction Partner: PSME3, MDFI, RBPMS, GLIS2, HSCB, FHOD1, EXOC7, PAX2, KRT18, EPAS1, EEF1A1, BHMT, ALDOB, UBC, UBD,
Protein Size: 721 -
分子量
- 80 kDa
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基因ID
- 583
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NCBI登录号
- NM_031885, NP_114091
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UniProt
- Q9BXC9
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途径
- Hedgehog Signaling
抗原
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