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Mouse Anti-TSPAN7 Recombinant Antibody (CBYJT-5083) (CBMAB-T4661-YJ)

Provided herein is a Mouse monoclonal antibody, which binds to TSPAN7 (Tetraspanin 7). The antibody can be used for immunoassay techniques, such as WB, IHC, IHC-P.
See all TSPAN7 antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
CBYJT-5083
Antibody Isotype
IgG1
Application
WB, IHC, IHC-P

Basic Information

Immunogen
This antibody was developed against a recombinant protein corresponding to amino acids: TFLRTYTDAMQTYNGNDERSRAVDHVQRSLSCCGVQNYTNWSTSPYFLEHGIPPSCCMNETDCNPQDLHNLTVAATKVNQKGCYDLVTSFMET
Specificity
Human
Antibody Isotype
IgG1
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Buffer
PBS, pH 7.4
Storage
Store at 4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
TSPAN7 Gene(Protein Coding)


Tetraspanin 7
Introduction
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. It mediate signal transduction events that function in the regulation of cell development, activation, growth and motility. TSPAN7 is a cell surface glycoprotein and may have a role in the control of neurite outgrowth. It is known to complex with integrins. TSPAN7 is associated with X-linked cognitive disability and neuropsychiatric diseases such as Huntington's chorea, fragile X syndrome and myotonic dystrophy.
Entrez Gene ID
7102
UniProt ID
P41732
Alternative Names
Tetraspanin 7; Transmembrane 4 Superfamily Member 2; Membrane Component Chromosome X Surface Marker 1; Cell Surface Glycoprotein A15; CD231 Antigen; DXS1692E; Tspan-7; TALLA-1; TM4SF2; MXS1; A15; T-Cell Acute Lymphoblastic Leukemia Associated Antigen 1
Function
May be involved in cell proliferation and cell motility.
Cellular Location
Membrane
Involvement in disease
Intellectual developmental disorder, X-linked 58 (XLID58):
A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. Intellectual deficiency is the only primary symptom of non-syndromic X-linked intellectual disability, while syndromic intellectual disability presents with associated physical, neurological and/or psychiatric manifestations.
Topology
Cytoplasmic: 1-16
Helical: 17-40
Extracellular: 41-56
Helical: 57-75
Cytoplasmic: 76-86
Helical: 87-112
Extracellular: 113-213
Helical: 214-234
Cytoplasmic: 235-249
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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