Recombinant Inhibin, alpha (INHA) (Gonadal Cell Marker) Antibody, Clone: [INHA/6598R], Rabbit, Monoclonal

Catalog Number: NBT-3623-RBM8-P1ABX
Article Name: Recombinant Inhibin, alpha (INHA) (Gonadal Cell Marker) Antibody, Clone: [INHA/6598R], Rabbit, Monoclonal
Biozol Catalog Number: NBT-3623-RBM8-P1ABX
Supplier Catalog Number: 3623-RBM8-P1ABX
Alternative Catalog Number: NBT-3623-RBM8-P1ABX-100
Manufacturer: NeoBiotechnologies
Host: Rabbit
Category: Antikörper
Application: IHC, WB
Species Reactivity: Human
Immunogen: Recombinant fragment of human Inhibin alpha protein (around aa 233-362) (exact sequence is proprietary)
Alternative Names: A inhibin subunit, IHA, inhA, Inhibin alpha chain, Inhibin alpha subunit
It recognizes a 47kDa protein, which is identified as alpha sub-unit of Inhibin. It is a gonadal protein that preferentially suppresses the secretion of pituitary follicle-stimulating hormone (FSH). Inhibin comprises two subunits, Inhibin A and Inhibin B. Each subunit consists of the same (TM) subunit, covalently linked to 1 of 2 distinct subunits, A°a-(TM) or A°a-A°a. Originally isolated from ovarian follicular fluid and characterized as a disulphide-linked dimeric glycoprotein, inhibin belongs to the transforming growth factor A°a (TFGA°a) superfamily. Antibodies against Inhibin are useful in making a differentiation between adrenal cortical tumors and renal cell carcinoma. Sex cord stromal tumors of the ovary as well as trophoblastic tumors also demonstrate cytoplasmic positivity. Inhibin antibody is also used to make the differential diagnosis of intra-uterine vs. ectopic pregnancy in endometrial curetting.
Clonality: Monoclonal
Clone Designation: [INHA/6598R]
Molecular Weight: 47kDa
NCBI: 3623
UniProt: P05111
Form: 200ug/ml of Ab purified from Bioreactor Concentrate by Protein A/G. Prepared in 1mM PBS with 0.05% BSA & 0.05% azide. Also available WITHOUT BSA & azide at 1.0mg/ml.
Antibody Type: Recombinant Monoclonal Antibody
Application Notes: Immunohistochemistry (Formalin-fixed) (1-2ug/ml for 30 minutes at RT),(Staining of formalin-fixed tissues requires heating tissue sections in 10mM Tris with 1mM EDTA, pH 9.0, for 45 min at 95 &degC followed by cooling at RT for 20 minutes),Optimal diluti
IHC analysis of formalin-fixed, paraffin-embedded hum