IFT172 Antibody, FITC conjugated

Code CSB-PA887019LC01HU
Size US$299
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Product Details

Full Product Name Rabbit anti-Homo sapiens (Human) IFT172 Polyclonal antibody
Uniprot No. Q9UG01
Target Names IFT172
Alternative Names IF172_HUMAN antibody; ift172 antibody; Intraflagellar transport 172 homolog (Chlamydomonas) antibody; Intraflagellar transport protein 172 homolog antibody; Osm 1 antibody; Selective LIM binding factor homolog antibody; SLB antibody; Wim antibody; Wimple homolog antibody
Raised in Rabbit
Species Reactivity Human
Immunogen Recombinant Human Intraflagellar transport protein 172 homolog protein (1368-1502AA)
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
Tested Applications ELISA
Protocols ELISA Protocol
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.

Target Data

Function Required for the maintenance and formation of cilia. Plays an indirect role in hedgehog (Hh) signaling, cilia being required for all activity of the hedgehog pathway (By similarity).
Gene References into Functions
  1. This is the second report of IFT172 mutations in BBS patients validating IFT172 as the twentieth BBS gene (BBS20). PMID: 26763875
  2. Findings identified mutations in IFT172 that lead to a recessive form of non-syndromic retinitis pigmentosa and Bardet-Biedl syndrome and suggest that the primary IFT172 mutations alone are not sufficient to explain the wide range of phenotypes. PMID: 25168386
  3. We have identified defects in IFT172 as a cause of complex asphyxiating thoracic dystrophy and Mainzer-Saldino syndrome. PMID: 24140113
Involvement in disease Short-rib thoracic dysplasia 10 with or without polydactyly (SRTD10); Retinitis pigmentosa 71 (RP71)
Subcellular Location Cell projection, cilium
Protein Families IFT172 family
Database Links

HGNC: 30391

OMIM: 607386

KEGG: hsa:26160

STRING: 9606.ENSP00000260570

UniGene: Hs.127401

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