IFT52 Antibody

Code CSB-PA896883LA01HU
Size US$166
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  • Western Blot
    Positive WB detected in: A549 whole cell lysate, HepG2 whole cell lysate, PC-3 whole cell lysate
    All lanes: IFT52 antibody at 5.1µg/ml
    Secondary
    Goat polyclonal to rabbit IgG at 1/50000 dilution
    Predicted band size: 50 kDa
    Observed band size: 50 kDa

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) IFT52 Polyclonal antibody
Uniprot No.
Target Names
IFT52
Alternative Names
IFT52 antibody; C20orf9 antibody; NGD5 antibody; CGI-53 antibody; Intraflagellar transport protein 52 homolog antibody; Protein NGD5 homolog antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human Intraflagellar transport protein 52 homolog protein (325-434AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated

The IFT52 Antibody (Product code: CSB-PA896883LA01HU) is Non-conjugated. For IFT52 Antibody with conjugates, please check the following table.

Available Conjugates
Conjugate Product Code Product Name Application
HRP CSB-PA896883LB01HU IFT52 Antibody, HRP conjugated ELISA
FITC CSB-PA896883LC01HU IFT52 Antibody, FITC conjugated
Biotin CSB-PA896883LD01HU IFT52 Antibody, Biotin conjugated ELISA
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
Tested Applications
ELISA, WB
Recommended Dilution
Application Recommended Dilution
WB 1:500-1:5000
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.
Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Function
Involved in ciliogenesis as part of a complex involved in intraflagellar transport (IFT), the bi-directional movement of particles required for the assembly, maintenance and functioning of primary cilia. Required for the anterograde transport of IFT88.
Gene References into Functions
  1. The data identify a new locus for short-rib polydactyly syndromes (SRPS) and show that IFT52 mutations result in a ciliopathy with primary effects on the skeleton. PMID: 27466190
  2. Whole-exome sequencing revealed a homozygous nonsense variant p.R142* in IFT52 encoding an IFT-B core complex protein as the probable cause of her condition. This is the first report of a human disease associated with IFT52 PMID: 26880018
Involvement in disease
Short-rib thoracic dysplasia 16 with or without polydactyly (SRTD16)
Subcellular Location
Cell projection, cilium.
Database Links

HGNC: 15901

OMIM: 617094

KEGG: hsa:51098

STRING: 9606.ENSP00000362121

UniGene: Hs.444332

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