|Application ||WB, E|
|Other Accession||NP_064425.2, NP_001001290.1|
|Calculated MW||58702 Da|
|Antigen Region||75-104 aa|
|Other Names||Solute carrier family 2, facilitated glucose transporter member 9, Glucose transporter type 9, GLUT-9, SLC2A9, GLUT9|
|Target/Specificity||This SLC2A9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 75-104 amino acids from the N-terminal region of human SLC2A9.|
|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||SLC2A9 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||Transport urate and fructose. May have a role in the urate reabsorption by proximal tubules. Also transports glucose at low rate.|
|Cellular Location||Isoform 1: Basolateral cell membrane; Multi- pass membrane protein|
|Tissue Location||Most strongly expressed in basolateral membranes of proximal renal tubular cells, liver and placenta Also detected in lung, blood leukocytes, heart skeletal muscle and chondrocytes from articular cartilage. Isoform 2 is only detected in the apical membranes of polarized renal tubular cells and placenta. Isoform 1 and isoform 2 are detected in kidney membrane (at protein level).|
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Provided below are standard protocols that you may find useful for product applications.
This gene encodes a member of the SLC2A facilitative glucose transporter family. Members of this family play a significant role in maintaining glucose homeostasis. The encoded protein may play a role in the development and survival of chondrocytes in cartilage matrices. Two transcript variants encoding distinct isoforms have been identified for this gene.
Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :
Facheris, M.F., et al. J. Mol. Neurosci. (2010) In press :
Houlihan, L.M., et al. Hum. Mol. Genet. 19(11):2321-2330(2010)
Urano, W., et al. Ann. Rheum. Dis. 69(5):932-933(2010)
Tabara, Y., et al. Am. J. Nephrol. 32(3):279-286(2010)
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