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The antibody against IGSF3 was raised in rabbit using the Recombinant Human Immunoglobulin superfamily member 3 protein (111-399aa) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB.
The antibody against IGSF3 was raised in rabbit using the Recombinant Human Immunoglobulin superfamily member 3 protein (111-399aa) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB.
$299.00
| Cat.No | ADC-55066A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | IGSF3 |
| Target Synonyms | EWI3 KIAA0466, IGSF3, Immunoglobulin superfamily member 3 (IgSF3) (Glu-Trp-Ile EWI motif-containing protein 3) (EWI-3) | Form | Liquid |
| Species Reactivity | Human | Isotype | IgG |
| Storage Buffer | 0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4 | Purification Method | >95%, Protein G purified |
| Conjugate | Non-conjugated | Application | ELISA, WB |
| Storage | Upon receipt |
| Immunogen Description | Recombinant Human Immunoglobulin superfamily member 3 protein (111-399aa) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | O75054 |
Uniprot Id
O75054
Target Species
Human
Target Name
IGSF3
Target Full Name
Immunoglobulin superfamily member 3
Target Involvement
Lacrimal duct defect (LCDD)
Target Subcellular Location
Membrane; Single-pass type I membrane protein.
Target Tissue Specificity
Expressed in a wide range of tissues with High expression in Placenta, kidney and lung.
Target Synonyms
IGSF3; EWI3; KIAA0466Immunoglobulin superfamily member 3; IgSF3; Glu-Trp-Ile EWI motif-containing protein 3; EWI-3
Target Background
The protein encoded by this gene is an immunoglobulin-like membrane protein containing several V-type Ig-like domains. A mutation in this gene has been associated with bilateral nasolacrimal duct obstruction (LCDD).
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