CLTCL1 (NM_007098) Human Recombinant Protein
Product Specifications
Background
This gene is a member of the clathrin heavy chain family and encodes a major protein of the polyhedral coat of coated pits and vesicles. Chromosomal aberrations involving this gene are associated with meningioma, DiGeorge syndrome, and velo-cardio-facial syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2009]
Synonyms
CHC22; CLH22; CLTCL; CLTD
Gene ID
8218
UniProt
P53675
Accession Number mRNA
NM_007098
Chromosomal Location
22q11.21
Expression System
HEK293T
Tag
C-Myc/DDK
Related Pathways
Endocytosis, Huntington's disease, Lysosome
Field of Research
Endocytosis, Huntington's disease, Lysosome
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Function
Druggable Genome
Molecular Weight
186.9 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
CLTCL1
Species
Human
Protein ID
NP_009029
Overview
Recombinant protein of human clathrin, heavy chain-like 1 (CLTCL1)
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/8218
Uniprot URL
https://www.uniprot.org/uniprot/P53675
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_007098
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_009029
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