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Cystinosis, Nephropathic (CTNS) ELISA Kits

CTNS encodes a seven-transmembrane domain protein that functions to transport cystine out of lysosomes. Additionally we are shipping CTNS Antibodies (44) and CTNS Proteins (8) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
CTNS 365969 Q9WTR6
CTNS 1497 O60931
Anti-Rat CTNS CTNS 287478  
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Top CTNS ELISA Kits at antibodies-online.com

Showing 3 out of 3 products:

Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Mouse
96 Tests Log in to see 11 to 13 Days
$875.60
Details
Human
96 Tests Log in to see 11 to 13 Days
$875.60
Details
Cow
96 Tests Log in to see 11 to 13 Days
$1,029.60
Details

More ELISA Kits for CTNS Interaction Partners

Mouse (Murine) Cystinosis, Nephropathic (CTNS) interaction partners

  1. Data indicate that hematopoietic stem cell (HSC (show FUT1 ELISA Kits)) transplantation in cystinosin knockout (Ctns-/-) thyroid drastically decreased cystine accumulation and normalized the thyroid-stimulating hormone level.

  2. Cells and tissues lacking CTNS expression are characterized by increased autophagosome numbers, but functional macroautophagic flux.

  3. The Ctns(-/-) mouse model generated on C57BL/6 background is not suitable for clarifying the pathogenesis of male infertility in cystinosis.

  4. Deletion of cystinosis gene (Ctns) causes corneal cystine crystals formation, neovascularization and scarring in the cornea of ctns transgenic mice mimicking cystinosis in humans.

  5. the cause of cellular ATP depletion in nephrotic cystinosis may be the futile cycle (show LRMP ELISA Kits), formed between two ATP-dependant gamma-glutamyl cycle enzymes, gamma-glutamyl cysteine synthetase and 5-oxoprolinase (show OPLAH ELISA Kits)

  6. CTNS has a role in proper functioning of the retina and bones, and in mouse behavior

  7. Temporospatial pattern of cystine accumulation in Ctns-/- mice parallels that of patients and validates the mice as a model for the ocular anomalies of cystinosis.

Human Cystinosis, Nephropathic (CTNS) interaction partners

  1. cystinosin-deficient cells had abnormal shape and distribution of the endo-lysosomal compartments and impaired endocytosis, with decreased surface expression of multiligand receptors and delayed lysosomal cargo processing.

  2. CTNS-LKG represents 5-20 % of CTNS transcripts, with the exception of the testis that expresses both isoforms in equal proportions.

  3. identified two novel CTNS splicing deletions in a Chinese IC family, one at the donor site of exon 6 of CTNS and the other at the acceptor site of exon 8

  4. We recommend that black South African and Cape Coloured patients presenting with cystinosis be tested for CTNS-c.971-12G > A in the first instance, with the possibility of prenatal testing being offered to at-risk families.

  5. Cystinosin, MPDU1, SWEETs and KDELR belong to a well-defined protein family with putative function of cargo receptors.[cytonosin]

  6. results objectify the pigmentation defect in patients with cystinosis. We also identify the role of CTNS in melanogenesis and add a new gene to the list of the genes involved in the control of skin and hair pigmentation

  7. Mutation analysis of CTNS in six cystinosis patients from four families in Thailand. Using PCR sequencing of the entire coding regions, study identified all eight mutant alleles, including two mutations, p.G309D and p.Q284X, that have not been previously reported.

  8. Report CTNS mutations in Turkish cystinosis patients.

  9. cystinosin exports the proteolysis-derived dimeric amino acid cystine from lysosomes and is impaired in cystinosis.

  10. CTNS plays a pivotal role in regulating cell thiol concentrations.

CTNS Antigen Profile

Antigen Summary

This gene encodes a seven-transmembrane domain protein that functions to transport cystine out of lysosomes. Its activity is driven by the H+ electrochemical gradient of the lysosomal membrane. Mutations in this gene cause cystinosis, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants.

Gene names and symbols associated with CTNS

  • solute carrier family 7 (cationic amino acid transporter, y+ system), member 11 (Slc7a11) antibody
  • cystinosin, lysosomal cystine transporter (CTNS) antibody
  • cystinosin, lysosomal cystine transporter (ctns) antibody
  • cystinosis, nephropathic (CTNS) antibody
  • cystinosis, nephropathic (ctns) antibody
  • cystinosin, lysosomal cystine transporter (Ctns) antibody
  • cystinosis, nephropathic (Ctns) antibody
  • 9930009M05Rik antibody
  • AI195360 antibody
  • AI451155 antibody
  • AW049661 antibody
  • CTNS antibody
  • CTNS-LSB antibody
  • PQLC4 antibody
  • sut antibody
  • xCT antibody
  • zgc:110194 antibody

Protein level used designations for CTNS

amino acid transport system xc- , cysteine/glutamate transporter , cystine/glutamate transporter , sodium independent anionic amino acid transport system , solute carrier family 7 member 11 , cystinosis, nephropathic , cystinosin , cystinosin-like , cystinosin, lysosomal cystine transporter

GENE ID SPECIES
365969 Mus musculus
417606 Gallus gallus
431937 Xenopus laevis
491220 Canis lupus familiaris
553594 Danio rerio
706721 Macaca mulatta
748043 Pan troglodytes
780074 Xenopus (Silurana) tropicalis
100060554 Equus caballus
100223329 Taeniopygia guttata
100409361 Callithrix jacchus
100443212 Pongo abelii
100592953 Nomascus leucogenys
1497 Homo sapiens
613527 Bos taurus
287478 Rattus norvegicus
83429 Mus musculus
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