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- 抗原 See all BBS2 抗体
- BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
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适用
- 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 BBS2 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human BBS2 (NP_114091.3).
- 亚型
- IgG
- Top Product
- Discover our top product BBS2 Primary Antibody
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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) (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
anti-Bardet-Biedl Syndrome 2 (BBS2) (N-Term) antibodyBBS2 适用: 人, 小鼠, 大鼠, 犬, Cow, 马, 兔, 斑马鱼, 豚鼠 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:500-1:2000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: 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. Avoid freeze / thaw cycles.
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- 抗原
- BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
- 别名
- BBS2 (BBS2 产品)
- 别名
- fb80a05 antibody, wu:fb80a05 antibody, DKFZp468B105 antibody, DKFZp469L0919 antibody, BBS antibody, 2410125H22Rik antibody, AI447581 antibody, Bardet-Biedl syndrome 2 antibody, bardet-biedl syndrome 2 antibody, Bardet-Biedl syndrome 2 (human) antibody, bbs2 antibody, BBS2 antibody, Bbs2 antibody
- 背景
- 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 seven other BBS proteins.
- 分子量
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Observed_MW: 100 kDa
Calculated_MW: 79 kDa
- 基因ID
- 583
- UniProt
- Q9BXC9
- 途径
- Hedgehog Signaling
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