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Cystinosin (CTNS, CTNS-LSB, PQLC4)

Cat no: C9070-50


Supplier: United States Biological
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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. Applications: Suitable for use in ELISA and Immunohistochemistry. Other applications not tested. Recommended Dilutions: ELISA: 1:1-1:1000 Immunohistochemistry (Paraffin): 1.25ug/ml. Validated for use on a panel of 21 formalin-fixed, paraffin-embedded human tissues after heat induced antigen retrieval in pH 6.0 citrate buffer. After incubation with C9070-50, slides were incubated with biotinylated Gt xRb IgG secondary antibody, followed by alkaline phosphatase-streptavidin and chromogen. Optimal dilutions to be determined by the researcher. Storage and Stability: May be stored at 4 degrees C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degrees C. Aliquots are stable for 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Catalogue number: C9070-50
Reactivities: Human
Hosts: Rabbit
Applications: ELISA, Immunohistochemistry
Size: 50ug
Form: Supplied as a liquid in PBS, 0.09% sodium azide.
P type: Pab
Isotype: IgG
Purity: Purified by Protein G affinity chromatography.
Additional info: Recognizes aa268-285 of human Cystinosin.

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