RSPH9 Antibody, FITC conjugated

Code CSB-PA867129LC01HU
Size US$166
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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) RSPH9 Polyclonal antibody
Uniprot No.
Target Names
RSPH9
Alternative Names
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
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human Radial spoke head protein 9 homolog protein (62-171AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
FITC
Clonality
Polyclonal
Isotype
IgG
Purification Method
>95%, Protein G purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Form
Liquid
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
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.

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Target Background

Function
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.
Gene References into Functions
  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
Involvement in disease
Ciliary dyskinesia, primary, 12 (CILD12)
Subcellular Location
Cytoplasm, cytoskeleton, cilium axoneme. Cell projection, cilium, flagellum. Cell projection, kinocilium.
Protein Families
Flagellar radial spoke RSP9 family
Database Links

HGNC: 21057

OMIM: 612648

KEGG: hsa:221421

UniGene: Hs.534585

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