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Mouse Anti-TACSTD2 Recombinant Antibody (CBT2103) (V2LY-0625-LY1664)

Tested Data

Summary

Host Animal
Mouse
Specificity
Human
Clone
CBT2103
Antibody Isotype
IgG2b
Application
WB, IHC, FC

Basic Information

Immunogen
Purified recombinant fragment of human TACSTD2 (AA: Extra(27-274)) expressed in E. Coli.
Host Species
Mouse
Specificity
Human
Antibody Isotype
IgG2b
Clonality
Monoclonal Antibody
Application Notes
ApplicationNote
WB1:500-1:2,000
IHC-P1:200-1:1,000
FC1:200-1:400
ELISA1:10,000

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

Format
Liquid
Buffer
PBS
Preservative
Sodium azide
Concentration
Batch dependent
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Entrez Gene ID
Function
May function as a growth factor receptor.
Biological Process
Biological Process negative regulation of branching involved in ureteric bud morphogenesisISS:UniProtKB
Biological Process negative regulation of cell motilityISS:UniProtKB
Biological Process negative regulation of epithelial cell migrationISS:UniProtKB
Biological Process negative regulation of ruffle assemblyISS:UniProtKB
Biological Process negative regulation of stress fiber assemblyISS:UniProtKB
Biological Process negative regulation of substrate adhesion-dependent cell spreadingISS:UniProtKB
Biological Process positive regulation of stem cell differentiationIBA:GO_Central1 Publication
Biological Process regulation of epithelial cell proliferationIEA:Ensembl
Biological Process response to stimulusIEA:UniProtKB-KW
Biological Process ureteric bud morphogenesisIEA:Ensembl
Biological Process visual perceptionTAS:ProtInc1 Publication
Cellular Location
Membrane
Involvement in disease
Corneal dystrophy, gelatinous drop-like (GDLD):
A form of lattice corneal dystrophy, a class of inherited stromal amyloidoses characterized by pathognomonic branching lattice figures in the cornea. GDLD is an autosomal recessive disorder characterized by severe corneal amyloidosis leading to blindness. Clinical manifestations, which appear in the first decade of life, include blurred vision, photophobia, and foreign-body sensation. By the third decade, raised, yellowish-gray, gelatinous masses severely impair visual acuity.
Topology
Extracellular: 27-274
Helical: 275-297
Cytoplasmic: 298-323
PTM
The N-terminus is blocked.
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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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