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- 抗原 See all BBS10 抗体
- BBS10 (Bardet-Biedl Syndrome 10 (BBS10))
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抗原表位
- AA 474-723
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适用
- 人
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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 BBS10 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- AENKDALEKT QTYLKVHSNL VIPDVELETY IPYSTPTLTP TDTFQTVETL TCLSLERNRL TDYYEPLLKN NSTAYSTRGN RIEISYENLQ VTNITRKGSM LPVSCKLPNM GTSQSYLSSS MPAGCVLPVG GNFEILLHYY LLNYAKKCHQ SEETMVSMII ANALLGIPKV LYKSKTGKYS FPHTYIRAVH ALQTNQPLVS SQTGLESVMG KYQLLTSVLQ CLTKILTIDM VITVKRHPQK VHNQDSEDEL
- 交叉反应
- 人, 小鼠
- 产品特性
- Polyclonal Antibodies
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 474-723 of human BBS10 (NP_078961.3).
- 亚型
- IgG
- Top Product
- Discover our top product BBS10 Primary Antibody
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anti-Bardet-Biedl Syndrome 10 (BBS10) (Internal Region) antibody
BBS10 适用: 人, 小鼠, 斑马鱼 WB, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 10 (BBS10) antibodyBBS10 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 10 (BBS10) (AA 515-544), (C-Term) antibodyBBS10 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB24715 unconjugated
anti-Bardet-Biedl Syndrome 10 (BBS10) (C-Term) antibodyBBS10 适用: 人, 兔 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB,1:200 - 1:3000
- 说明
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HIGH QUALITY
- 限制
- 仅限研究用
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- 状态
- Liquid
- 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
- BBS10 (Bardet-Biedl Syndrome 10 (BBS10))
- 别名
- BBS10 (BBS10 产品)
- 别名
- MGC84945 antibody, si:dkey-30c15.16 antibody, C12orf58 antibody, RGD1560748 antibody, 1300007O09Rik antibody, AI452285 antibody, Bardet-Biedl syndrome 10 antibody, Bardet-Biedl syndrome 10 L homeolog antibody, Bardet-Biedl syndrome 10 (human) antibody, BBS10 antibody, bbs10.L antibody, bbs10 antibody, Bbs10 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 progressive retinal degeneration, 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 is likely not a ciliary protein but rather has distant sequence homology to type II chaperonins. As a molecular chaperone, this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes. Mutations in this gene cause Bardet-Biedl syndrome type 10.,BBS10,C12orf58,Epigenetics & Nuclear Signaling,Transcription Factors,Neuroscience,BBS10
- 分子量
- 80 kDa
- 基因ID
- 79738
- UniProt
- Q8TAM1
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