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Antigenic Specificity | GCDFP-15, Human |
Clone | REAL828 |
Host Species | Recombinant Human |
Reactive Species | human |
Isotype | n/a |
Format | fluorescein (FITC) conjugate |
Size | 200 µL |
Concentration | n/a |
Applications | MICS (MACSima Imaging Cyclic Staining), Immunohistochemistry, Immunofluorescence |
Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
Description | GCDFP-15 Antibody, anti-human, FITC, REAdye_lease™. Clone REAL828 is an antibody fragment derived from the full GCDFP-15 antibody molecule. It displays no binding to Fc receptors. The recombinantly engineered antibody fragments are multimerized to form the REAdye_lease Complex to bind markers with high avidity. | Clone REAL828 recognizes the GCDFP-15 (gross cystic disease fluid protein 15), also known as Prolactin-inducible protein, extra-parotid glycoprotein (EP-GP), gp17 seminal actin-binding protein (SABP) or BRST2. In humans it is encoded by the PIP gene and is upregulated by prolactin and androgens and downregulated by estrogen. GCDFP-15 has various physiological functions and is used as a detection and diagnostic marker of breast cancer cells. | For removal of REAdye_lease fluorochromes for optional relabeling with different fluorochrome-conjugated REAdye_lease antibodies use the REAlease Support Kit (130-120-675). |
Immunogen | n/a |
Other Names | PIP, GCDFP15, GPIP4, prolactin induced protein, extra-parotid glycoprotein (EP-GP), gp17 seminal actin-binding protein (SABP), BRST2 |
Gene, Accession # | n/a |
Catalog # | 130-126-210 |
Price | $355 |
Order / More Info | GCDFP-15, Human Antibody from MILTENYI BIOTEC B.V. & Co. KG |
Product Specific References | Naderi, A. et al. (2012) Prolactin-induced protein mediates cell invasion and regulates integrin signaling in estrogen receptor-negative breast cancer. Breast Cancer Res. 14 (4): R111. | Urbaniak, A. et al. (2018) Prolactin-induced protein (PIP)-characterization and role in breast cancer progression. Am. J. Cancer Res. 8 (11): 2150-2164. |