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.

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