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May be important in developing and maintaining corneal transparency and for the structure of the stromal matrix. Additionally we are shipping Keratocan Kits (13) and Keratocan Proteins (5) and many more products for this protein.
Showing 10 out of 45 products:
Human Polyclonal KERA Primary Antibody for ELISA, WB - ABIN564810
Zhang, Conrad, Conrad: Effects of ultraviolet-A and riboflavin on the interaction of collagen and proteoglycans during corneal cross-linking. in The Journal of biological chemistry 2011
Show all 2 references for ABIN564810
Human Polyclonal KERA Primary Antibody for EIA, WB - ABIN953035
Aldave, Rosenwasser, Yellore, Papp, Sobel, Pham, Chen, Dandekar, Sripracha, Rayner, Sassani, Gorin: Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC. in Investigative ophthalmology & visual science 2010
Human Polyclonal KERA Primary Antibody for IHC, IHC (p) - ABIN4328604
Syed-Picard, Du, Lathrop, Mann, Funderburgh, Funderburgh: Dental pulp stem cells: a new cellular resource for corneal stromal regeneration. in Stem cells translational medicine 2015
Human Polyclonal KERA Primary Antibody for WB - ABIN656548
Wheeler, Metter, Tanaka, Absher, Higgins, Zahn, Wilhelmy, Davis, Singleton, Myers, Ferrucci, Kim: Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging. in PLoS genetics 2009
Data indicate that mammalian keratocan is conserved in zebrafish in terms of gene structure, expression pattern, and promoter function.
rare variant in KERA was identified in a large kindred with premature atherosclerosis
our results demonstrate the expression of keratocan by osteoblast lineage cells and its ability to modulate osteoblast function.
Keratocan plays a unique role in maintaining the appropriate corneal shape to ensure normal vision
Keratocan-deficient mice have corneal collagen fibrils with significantly larger diameters than those in wild-type mice, and increased centre-to-centre spacing of the fibrils.
lumican (show LUM Antibodies) has a novel regulatory role in keratocan expression at the transcriptional level
lumican (show LUM Antibodies) and keratocan core proteins bind the CXC chemokine (show CXCL12 Antibodies) KC during a corneal inflammatory response, indicating that corneal KSPGs mediate neutrophil recruitment to the cornea by regulating chemokine (show CCL1 Antibodies) gradient formation.
The mutation that we report here leads to the deletion of a conserved amino acid (p.Phe125del) from the third LRR motif of the keratocan protein, which might lead to an abnormal tertiary structure of the protein, thereby leading to the disease.
a novel KERA variant, p.(Ile225Thr), was detected that segregates with Cornea plana in the homozygous form.
Corneal endothelial disorders were found with compound mutations in KERA
Linkage and haplotype analyses identified 12q21.33 as a locus for posterior amorphous corneal dystrophy. However, no mutations were identified in the candidate genes (KERA, LUM (show LUM Antibodies), DCN (show DCN Antibodies), EPYC (show EPYC Antibodies)) within this region.
KERA mutation is associated with autosomal recessive cornea plana
This is the first report of the identification of a mutation within KERA in a family of Hispanic origin with autosomal recessive cornea plana.
No evidence that endothelial dysfunction and germline mutation of lumican and keratocan genes participate in the etiology of subepithelial corneal haze.
Specific for mutation in KERA, the ophthalmic phenotype of recessive cornea plana does not significantly vary with different KERA mutations.
In addition, no pathogenic sequence variations were found in DCN (show DCN Antibodies), DSPG3 (show EPYC Antibodies), LUM (show LUM Antibodies), PITX2 (show PITX2 Antibodies) and FOXC1 (show FOXC1 Antibodies), which have also been implicated in corneal and anterior segment dysgenesis.
FGF-2 (show FGF2 Antibodies)- and TGF-beta1 (show TGFB1 Antibodies)-activation of JNK (show MAPK8 Antibodies) signaling pathway may be partly responsible for the downregulation of keratocan and lumican (show LUM Antibodies) expression in activated corneal keratocytes observed during corneal stromal wound healing.
May be important in developing and maintaining corneal transparency and for the structure of the stromal matrix.
, keratan sulfate proteoglycan keratocan
, KSPG keratocan
, corneal keratan sulfate proteoglycan 37A core protein