MLC1 Antibody (C-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
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Application ![]()
| WB, E |
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Primary Accession | Q15049 |
Other Accession | Q60HE7, NP_055981.1 |
Reactivity | Human |
Predicted | Monkey |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 41141 Da |
Antigen Region | 337-366 aa |
Gene ID | 23209 |
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Other Names | Membrane protein MLC1, MLC1, KIAA0027, WKL1 |
Target/Specificity | This MLC1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 337-366 amino acids from the C-terminal region of human MLC1. |
Dilution | WB~~1:1000 E~~Use at an assay dependent concentration. |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | MLC1 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | MLC1 (HGNC:17082) |
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Function | Transmembrane protein mainly expressed in brain astrocytes that may play a role in transport across the blood-brain and brain- cerebrospinal fluid barriers (PubMed:22328087). Regulates the response of astrocytes to hypo-osmosis by promoting calcium influx (PubMed:22328087). May function as regulatory protein of membrane protein complexes such as ion channels (Probable). |
Cellular Location | Membrane; Multi-pass membrane protein. Cell membrane; Multi-pass membrane protein. Cytoplasm, perinuclear region. Endoplasmic reticulum |
Tissue Location | Expressed in the brain, with highest levels found in the amygdala, nucleus caudatus, thalamus and hippocampus |
For Research Use Only. Not For Use In Diagnostic Procedures.
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
The function of this gene product is unknown; however, homology to other proteins suggests that it may be an integral membrane transporter. Mutations in this gene have been associated with megalencephalic leukoencephalopathy with subcortical cysts, an autosomal recessive neurological disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.
REFERENCES
Yis, U., et al. Turk. J. Pediatr. 52(2):179-183(2010)
Lanciotti, A., et al. Neurobiol. Dis. 37(3):581-595(2010)
Shukla, P., et al. Prenat. Diagn. 28(4):357-359(2008)
Ambrosini, E., et al. Mol. Cell. Neurosci. 37(3):480-493(2008)
Selch, S., et al. Biol. Psychiatry 61(10):1211-1214(2007)

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