Human Tetraspanin-7 (TSPAN7) ELISA Kit

Product specifications

ELISA Kits

Tetraspanin-7 (TSPAN7)

Human

Colorimetric

Quantitative

Sandwich

78 pg/ml - 5000 pg/ml

< 39 pg/ml

Optimal dilutions/concentrations should be determined by the end user.

96 tests

Lyophilized

ELISA

Tissue homogenates, cell lysates and other biological fluids.

Shipped within 5-12 working days. The validity for this kit is 6 months.

Shipped at 4 °C. Upon receipt, store the kit according to the storage instruction in the kit's manual.

No

P41732

Membrane component chromosome X surface marker 1,A15,MXS1,CD231, MRX58,CCG-B7,TM4SF2,XLID58,T-cell acute lymphoblastic leukemia-associated antigen 1,TALLA-1

Elisa kits for TSPAN7

RUO

Validity: The validity for this kit is 6 months.

This product is for research use only.   The range and sensitivity is subject to change. Please contact us for the latest product information. For accurate results, sample concentrations must be diluted to mid-range of the kit. If you require a specific range, please contact us in advance or write your request in your order comments.   Please note that our ELISA and CLIA kits are optimised for detection of native samples, rather than recombinant proteins. We are unable to guarantee detection of recombinant proteins, as they may have different sequences or tertiary structures to the native protein.

Descripción

Tetraspanin 7 (TSPAN7) is a member of the tetraspanin superfamily, a group of membrane proteins involved in various cellular functions such as signaling, adhesion, and intracellular trafficking. Tetraspanins are characterized by their distinctive structure, containing four transmembrane domains. TSPAN7 is primarily expressed in the central nervous system, particularly in neurons, and is also found in certain immune cells. TSPAN7 is of interest due to its involvement in neurological processes and its role in neurodevelopmental disorders, most notably X-linked intellectual disability (XLID). Mutations or dysregulation of TSPAN7 have been implicated in cognitive deficits, autism spectrum disorders, and other neurological conditions, highlighting its importance in normal brain function. The primary role of TSPAN7 appears to be in facilitating cell-cell interactions and maintaining synaptic function. Through its association with other proteins in the tetraspanin web—an organized network of tetraspanins and their partner proteins—TSPAN7 modulates cellular signaling pathways crucial for neuronal growth, differentiation, and communication. These functions make TSPAN7 essential for neural development and synaptic plasticity, processes that underlie learning and memory.

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TSPAN7 Antibody is a Rabbit Polyclonal antibody against TSPAN7. 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.

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