catalog number :
MBS9206828
products full name :
TSPAN7 Antibody (Center)
products short name :
[TSPAN7]
products name syn :
[Tetraspanin-7; Tspan-7; Cell surface glycoprotein A15; Membrane component chromosome X surface marker 1; T-cell acute lymphoblastic leukemia-associated antigen 1; TALLA-1; Transmembrane 4 superfamily member 2; CD231; TSPAN7; A15; DXS1692E; MXS1; TM4SF2]
other names :
[tetraspanin-7; Tetraspanin-7; tetraspanin-7; tetraspanin 7; Cell surface glycoprotein A15; Membrane component chromosome X surface marker 1; T-cell acute lymphoblastic leukemia-associated antigen 1; TALLA-1; Transmembrane 4 superfamily member 2; CD_antigen: CD231]
products gene name :
[TSPAN7]
other gene names :
[TSPAN7; TSPAN7; A15; MXS1; CD231; MRX58; CCG-B7; TM4SF2; TALLA-1; TM4SF2b; DXS1692E; A15; DXS1692E; MXS1; TM4SF2; Tspan-7; TALLA-1]
uniprot entry name :
TSN7_HUMAN
reactivity :
Human (Predicted Reactivity: Mouse)
sequence positions :
[98-124]
specificity :
This TSPAN7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 98-124 amino acids from the Central region of human TSPAN7.
purity :
Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)
form :
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 stability :
Maintain refrigerated at 2-8°C weeks for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
tested application :
Western Blot (WB), ELISA (EIA), Flow Cytometry (FC/FACS)
app notes :
WB~~1:1000. FC~~1:10~50
image1 heading :
Western Blot (WB)
image2 heading :
Flow Cytometry (FC/FACS)
other info1 :
Calculated MW: 27574
other info2 :
Function: May be involded in cell proliferation and cell motility. Cellular location: Membrane; Multi-pass membrane protein. Tissue location: Not solely expressed in T-cells. Expressed in acute myelocytic leukemia cells of some patients.
products categories :
Signal Transduction
products description :
TSPAN7 is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein and may have a role in the control of neurite outgrowth. It is known to complex with integrins. This gene is associated with X-linked mental retardation and neuropsychiatric diseases such as Huntington's chorea, fragile X syndrome and myotonic dystrophy.
products references :
Radhakrishnan, Y., et al. Biol. Reprod. 81(4):647-656(2009). Guilmatre, A., et al. Arch. Gen. Psychiatry 66(9):947-956(2009). Noor, A., et al. Psychiatr. Genet. 19(3):154-155(2009)
ncbi acc num :
NP_004606.2
ncbi gb acc num :
NM_004615.3
ncbi pathways :
Ubiquinone And Other Terpenoid-quinone Biosynthesis Pathway (7102); Ubiquinone And Other Terpenoid-quinone Biosynthesis Pathway (7102)
ncbi summary :
The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein and may have a role in the control of neurite outgrowth. It is known to complex with integrins. This gene is associated with X-linked mental retardation and neuropsychiatric diseases such as Huntington's chorea, fragile X syndrome and myotonic dystrophy. [provided by RefSeq, Jul 2008]
uniprot summary :
TSPAN7: a multi-pass membrane protein. Member of the transmembrane 4 superfamily, also known as the tetraspanin family. These proteins apparently mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. Defects in TSPAN7 are the cause of mental retardation X- linked type 58 (MRX58). Mental retardation is characterized by significantly sub-average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. Non-syndromic mental retardation patients do not manifest other clinical signs. Protein type: Membrane protein, integral; Membrane protein, multi-pass. Chromosomal Location of Human Ortholog: Xp11.4. Cellular Component: integral to plasma membrane. Biological Process: viral reproduction. Disease: Mental Retardation, X-linked 58