Recombinant Human L1CAM Protein (Met1-Glu1120), C-His tagged
Cat.No. : | L1CAM-4399H |
Product Overview : | Recombinant human L1CAM (Met1-Glu1120) fused with the C-terminal His tag was expressed in Mammalian cells. |
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Source : | Mammalian cells |
Species : | Human |
Tag : | His |
Form : | Lyophilized powder/frozen liquid |
Molecular Mass : | 123.2 kDa |
Protein length : | Met1-Glu1120 |
Endotoxin : | < 1.0 EU/μg of the protein as determined by the LAL method. |
Purity : | >90% as determined by SDS-PAGE. |
Notes : | For research use only. |
Storage : | Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8 centigrade for one week. Store at -20 to -80 centigrade for twelve months from the date of receipt. |
Storage Buffer : | Supplied as solution form in PBS or lyophilized from PBS. |
Reconstitution : | Reconstitute in sterile water for a stock solution. |
Shipping : | They are shipped out with dry ice/blue ice unless customers require otherwise. |
Gene Name : | L1CAM L1 cell adhesion molecule [ Homo sapiens (human) ] |
Official Symbol : | L1CAM |
Synonyms : | L1CAM; L1 cell adhesion molecule; antigen identified by monoclonal R1, HSAS, HSAS1, MASA, MIC5, S10, SPG1; neural cell adhesion molecule L1; CD171; antigen identified by monoclonal R1; S10; HSAS; MASA; MIC5; SPG1; CAML1; HSAS1; N-CAML1; NCAM-L1; N-CAM-L1; |
Gene ID : | 3897 |
mRNA Refseq : | NM_000425 |
Protein Refseq : | NP_000416 |
MIM : | 308840 |
UniProt ID : | P32004 |
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◆ Lysates | ||
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Not For Human Consumption!
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Customer Reviews (3)
Write a reviewL1CAM protein is an enzyme involved in the digestion of carbohydrates, specifically starch.
A reliable manufacturer ensures the production and purification of L1CAM protein, maintaining its quality and purity.
Manufacturers should provide detailed information about the production process, quality control measures, and purity assessment methods employed.
Q&As (5)
Ask a questionSome clinical trials are exploring L1CAM-targeted therapies in the context of cancer treatment.
L1CAM mutations can be diagnosed through genetic testing, aiding in the diagnosis of L1 syndrome and related conditions.
L1CAM has been explored as a potential therapeutic target for inhibiting tumor metastasis in some cancer types.
L1CAM is not typically associated with neurodegenerative diseases, but its role in neural development may have implications for regenerative medicine.
L1CAM has been associated with certain developmental disorders and cognitive deficits in addition to cancer and neurological disorders.
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