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The antibody against OSGIN1 was raised in rabbit using the Human OSGIN1 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.
The antibody against OSGIN1 was raised in rabbit using the Human OSGIN1 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.
$600.00
| Cat.No | ADC-47731A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | OSGIN1 |
| Form | Liquid | Species Reactivity | Human, Mouse, Rat |
| Isotype | IgG | Storage Buffer | 50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.02% sodium azide |
| Purification Method | Antigen affinity purified | Conjugate | Non-conjugated |
| Application | ELISA, WB | Storage | Upon receipt |
| Immunogen Description | Human OSGIN1 | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | Q9UJX0 |
Uniprot Id
Q9UJX0
Target Species
Human
Target Name
OSGIN1
Target Full Name
Oxidative stress-induced growth inhibitor 1
Target Function
Regulates the differentiation and proliferation through the regulation of cell death.
Target Protein Families
OKL38 family
Target Tissue Specificity
Ubiquitous. Highest expression in the ovary, testis, kidney, skeletal muscle and liver. Weakly expressed in spleen, heart, kidney, and pancreas. Highly expressed in tumor cells (at protein level).
Target Synonyms
OSGIN1; BDGI; OKL38; Oxidative stress-induced growth inhibitor 1; Bone marrow stromal cell-derived growth inhibitor; BMSC-derived growth inhibitor; Ovary; kidney and liver protein 38; huOKL38; Pregnancy-induced growth inhibitor OKL38
Target Background
This gene encodes an oxidative stress response protein that regulates cell death. Expression of the gene is regulated by p53 and is induced by DNA damage. The protein regulates apoptosis by inducing cytochrome c release from mitochondria. It also appears to be a key regulator of both inflammatory and anti-inflammatory molecules. The loss of this protein correlates with uncontrolled cell growth and tumor formation. Naturally occurring read-through transcription exists between this gene and the neighboring upstream malonyl-CoA decarboxylase (MLYCD) gene, but the read-through transcripts are unlikely to produce a protein product.
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