RSPH9 Antibody, FITC conjugated

Datasheet

Code	CSB-PA867129LC01HU
Size	US$166
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Product Details
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Target Background

Product Details

Full Product Name

Rabbit anti-Homo sapiens (Human) RSPH9 Polyclonal antibody

Uniprot No.

Q9H1X1

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

Antibody 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.

Usage

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

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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

Mutations in RSPH9 leads to ultrastructural cilia defects and ciliary dyskinesia. PMID: 22448264
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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Service

Phage Display Service

Antibody Service

Protein Service

Gene Synthesis Service

Oligo Synthesis Service

Antibody FAQs What Is an Antibody? How to Choose an Antibody for Scientific Research? The difference between primary antibody and secondary antibod The Meaning of Irregular Antibody Screening Tag Antibodies, Your Good Partner in Protein Research How to Choose the Loading Control Antibodies?

Call us

301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)

[email protected]

Address

7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA

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