RSPH9 Antibody, Biotin conjugated

产品详情

产品名称：

Rabbit anti-Homo sapiens (Human) RSPH9 Polyclonal antibody
Uniprot No.：

Q9H1X1
基因名：

RSPH9
别名：

C6orf206 antibody; Chromosome 6 open reading frame 206 antibody; CILD12 antibody; FLJ30845 antibody; Mitochondrial ribosomal protein S18A like 1 antibody; MRPS18AL1 antibody; Radial spoke head 9 homolog antibody; Radial spoke head protein 9 homolog antibody; RSPH 9 antibody; rsph9 antibody; RSPH9_HUMAN antibody; Uncharacterized protein C6orf206 antibody
宿主：

Rabbit
反应种属：

Human
免疫原：

Recombinant Human Radial spoke head protein 9 homolog protein (62-171AA)
免疫原种属：

Homo sapiens (Human)
标记方式：

Biotin
克隆类型：

Polyclonal
抗体亚型：

IgG
纯化方式：

>95%, Protein G purified
浓度：

It differs from different batches. Please contact us to confirm it.
保存缓冲液：

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
产品提供形式：

Liquid
应用范围：

ELISA
Protocols：

ELISA Protocol
储存条件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
货期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

功能：

Component of the axonemal radial spoke head which plays an important role in ciliary motility. Essential for both the radial spoke head assembly and the central pair microtubule stability in ependymal motile cilia. Required for motility of olfactory and neural cilia and for the structural integrity of ciliary axonemes in both 9+0 and 9+2 motile cilia.
基因功能参考文献：
1. Mutations in RSPH9 leads to ultrastructural cilia defects and ciliary dyskinesia. PMID: 22448264
2. Study focused on an extended 5 generation Bedouin family, analysed mutation segregation, and calculated the age of the mutated allele in 2 families based on haplotypes and haplotype+microsatellite in an attempt to define the source of the mutation. PMID: 20070851
相关疾病：

Ciliary dyskinesia, primary, 12 (CILD12)
亚细胞定位：

Cytoplasm, cytoskeleton, cilium axoneme. Cell projection, cilium, flagellum. Cell projection, kinocilium.
蛋白家族：

Flagellar radial spoke RSP9 family
数据库链接：

HGNC: 21057

OMIM: 612648

KEGG: hsa:221421

UniGene: Hs.534585