Analytical Data
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Gene name
CCIN
- Application
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Alternative Names
CCINCalicin
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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
Q13939
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Expression Region
1-588aa
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AA Sequence
MKLEFTEKNYNSFVLQNLNRQRKRKEYWDMALSVDNHVFFAHRNVLAAVSPLVRSLISSNDMKTADELFITIDTSYLSPVTVDQLLDYFYSGKVVISEQNVEELLRGAQYFNTPRLRVHCNDFLIKSICRANCLRYLFLAELFELKEVSDVAYSGIRDNFHYWASPEGSMHFMRCPPVIFGRLLRDENLHVLNEDQALSALINWVYFRKEDREKYFKKFFNYINLNAVSNKTLVFASNKLVGMENTSSHTTLIESVLMDRKQERPCSLLVYQRKGALLDSVVILGGQKAHGQFNDGVFAYIIQENLWMKLSDMPYRAAALSATSAGRYIYISGGTTEQISGLKTAWRYDMDDNSWTKLPDLPIGLVFHTMVTCGGTVYSVGGSIAPRRYVSNIYRYDERKEVWCLAGKMSIPMDGTAVITKGDRHLYIVTGRWLVKGYISRVGVVDCFDTSTGDVVQCITFPIEFNHRPLLSFQQDNILCVHSHRQSVEINLQKVKASKTTTSVPVLPNSCPLDVSHAICSIGDSKVFVCGGVTTASDVQTKDYTINPNAFLLDQKTGKWKTLAPPPEALDCPACCLAKLPCKILQRI
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Molecular Weight
93.1 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
Related Products
Protein Description
CCIN, or the "Coiled-Coil Domain Containing Protein," has garnered significant attention in recent years due to its potential roles in various biological processes and diseases. Initially identified through genomic studies, CCIN exhibits a coiled-coil structural motif, which is known to mediate protein-protein interactions crucial for cellular functions such as signaling, structural support, and regulation of metabolic pathways. Research has indicated that CCIN may play a pivotal role in the development of certain cancers and inflammatory conditions, prompting scientists to explore its mechanisms and potential as a therapeutic target. Additionally, CCIN's unique properties make it an attractive candidate for the development of recombinant proteins, which are valuable in biotechnology and therapeutic applications. By producing CCIN as a recombinant protein, researchers aim to investigate its structure-function relationship, interactions with other proteins, and its implications in cellular processes. This research not only sheds light on the biological significance of CCIN but also opens avenues for novel treatment strategies and biotechnological innovations. Overall, the study of CCIN and its recombinant forms holds promise for advancing our understanding of complex diseases and enhancing protein-based therapeutic approaches.
