Recombinant Human GRIN1 protein, His-tagged
Cat.No. : | GRIN1-1905H |
Product Overview : | Recombinant Human GRIN1 protein(NP_015566.1)(Arg 19 - Gln 559), fused with His tag, was expressed in HEK293. |
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Source : | HEK293 |
Species : | Human |
Tag : | His |
Form : | PBS, pH7.4 |
Molecular Mass : | 62.4 kDa |
Protein Length : | Arg 19 - Gln 559 |
Endotoxin : | Less than 1.0 EU per μg by the LAL method. |
Purity : | >95% as determined by SDS-PAGE. |
Storage : | For long term storage, the product should be stored at lyophilized state at -20°C or lower. Please avoid repeated freeze-thaw cycles. This product is stable after storage at: -20°C to -70°C for 12 months in lyophilized state; -70°C for 3 months under sterile conditions after reconstitution. |
Reconstitution : | It is recommended that sterile water be added to the vial to prepare a stock solution of 0.2 ug/ul. Centrifuge the vial at 4°C before opening to recover the entire contents. |
Gene Name : | GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1 [ Homo sapiens ] |
Official Symbol : | GRIN1 |
Synonyms : | GRIN1; glutamate receptor, ionotropic, N-methyl D-aspartate 1; NMDAR1; glutamate [NMDA] receptor subunit zeta-1; GluN1; NMD-R1; glutamate [NMDA] receptor subunit zeta 1; N-methyl-D-aspartate receptor subunit NR1; N-methyl-D-aspartate receptor channel, subunit zeta-1; NR1; MRD8; NMDA1; |
Gene ID : | 2902 |
mRNA Refseq : | NM_000832 |
Protein Refseq : | NP_000823 |
MIM : | 138249 |
UniProt ID : | Q05586 |
Products Types
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Grin1-1064M | Recombinant Mouse Grin1 Protein, MYC/DDK-tagged | +Inquiry |
GRIN1-2361H | Recombinant Human GRIN1 Protein, MYC/DDK-tagged | +Inquiry |
GRIN1-1020H | Recombinant Human GRIN1 Protein, His (Fc)-Avi-tagged | +Inquiry |
◆ Lysates | ||
GRIN1-5745HCL | Recombinant Human GRIN1 293 Cell Lysate | +Inquiry |
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For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (5)
Ask a questionDysregulation of the NMDA receptor, due to GRIN1 mutations, has been linked to neurodegenerative diseases such as Alzheimer's and Parkinson's.
Disorders such as epilepsy, autism spectrum disorders, and schizophrenia have been linked to GRIN1 mutations.
Yes, genetic testing can identify mutations in the GRIN1 gene, which may be helpful in diagnosing certain neurological conditions.
The NMDA receptor, with GRIN1 as a subunit, is crucial for long-term potentiation, a process underlying memory formation and learning.
Some studies suggest that genetic variations in GRIN1 may influence an individual's response to antidepressant medications.
Customer Reviews (3)
Write a reviewThis strong track record of excellence further attests to the GRIN1 protein's capability to meet the rigorous demands of research projects.
Whether measuring analyte concentrations, screening for specific interactions, or monitoring immune responses, this protein's exceptional performance in ELISA experiments is truly commendable.
Its high quality, reliability, and exceptional performance make it an excellent choice for a wide range of experimental applications.
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