Analytical Data
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Gene name
C16orf71
- Application
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Alternative Names
C16orf71Uncharacterized Protein C16orf71
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Species
Human
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Source
E. coli
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Tag
GST-tag at N-terminal
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Purity
Greater than 90% as determined by SDS-PAGE.
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Uniprot
Q8IYS4
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Expression Region
1-520aa
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AA Sequence
MASNDKGMAP SLGSPWASQM GPWDAILKAV KDQLPSLDSD SPLSDYGEEE LFIFQRNQTS LIPDLSEELA EDPADGDKSR AWVAAAEESL PEPVLVPAEL ATEPGCRQNT RTKDASSQEG RDPGRPFESS GEVSALLGMA EEPPRWLEGD LGSLSFNTKG SQGPPWDPQA EATLSCHEGD PKAEPLSTAS QESVNRRALR QERRKMIETD ILQKVTRDAC GPTSSDKGGV KEAPCHAAES APRSKMPLVE PPEGPPVLSL QQLEAWDLDD ILQSLAGQED NQGNRAPGTV WWAADHRQVQ DRMVPSAHNR LMEQLALLCT TQSKASACAR KVPADTPQDT KEADSGSRCA SRKQGSQAGP GPQLAQGMRL NAESPTIFID LRQMELPDHL SPESSSHSSS DSEEEEEEEM AALGDAEGAS PSSLGLRTCT GKSQLLQQLR AFQKGTAQPE LPASKGPAGG RAQAPEDTAG SRTGRKQHMK LCAKGQSAQA RLPRGRPRAL GDVPEPGAAR EALMPPLEQL
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Molecular Weight
83.6 kDa
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Endotoxin
< 1.0 EU per μg protein as determined by the LAL method.
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Form
Freeze-dried powder
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Buffer formulation
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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Reconstitution
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- Customization
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Stability Test
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
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Storage & Shelf Life
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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Shipping
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
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Protein Description
C16orf71, a gene located on chromosome 16, has garnered significant attention in the field of molecular biology and genetics due to its potential role in various cellular processes and disease mechanisms. Research has indicated that mutations in C16orf71 are linked to retinal dystrophies and other syndromic conditions, highlighting its importance in vision and neurodevelopment. The study of recombinant C16orf71 protein is crucial for understanding its structure-function relationship, which may illuminate the pathways it influences and its interactions with other cellular proteins. To elucidate its biological role, researchers have focused on creating recombinant forms of C16orf71 to facilitate biochemical assays, structural analyses, and functional studies. This involves the expression of the protein in various systems, allowing for the characterization of its properties and the exploration of its involvement in signaling pathways and cellular functions. Understanding C16orf71 at the protein level not only holds promise for unraveling the etiology of associated diseases but also offers potential avenues for therapeutic interventions. As research advances, the insights gained from studies of recombinant C16orf71 may contribute to the development of targeted strategies to manage conditions linked to its dysfunction.
