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Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting immunostaining in relation to complex human pathologies.

Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding. Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".

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INHBA / Inhibin Beta A Antibody (aa85‑112) LS‑C165241
Inhibin Beta A antibody LS-C165241 is an unconjugated rabbit polyclonal antibody to human Inhibin Beta A (INHBA). Validated for Flow, IF, IHC and WB.
Catalog
Size
Price
LS-C165241-400
400 µl
Unavailable

Popular INHBA / Inhibin Beta A Products

Antibody
Species: Human, Mouse, Rat
Applications: Western blot, ELISA
Antibody
Species: Human
Applications: ELISA
Antibody
Species: Human
Applications: IHC, ICC, Immunofluorescence, Western blot, Flow Cytometry, ELISA
Antibody
Species: Human
Applications: IHC, ICC, Immunofluorescence, Western blot, Flow Cytometry, ELISA
Human Small Intestine: Formalin-Fixed, Paraffin-Embedded (FFPE).  This image was taken for the unconjugated form of this product. Other forms have not been tested.
Species: Human, Monkey, Mouse, Rat, Bovine, Goat, Hamster, Horse, Pig, Sheep
Applications: IHC, IHC - Paraffin, Western blot

Product Description

Inhibin Beta A antibody LS-C165241 is an unconjugated rabbit polyclonal antibody to human Inhibin Beta A (INHBA). Validated for Flow, IF, IHC and WB.
About INHBA / Inhibin Beta A
The inhibin beta A subunit joins the alpha subunit to form a pituitary FSH secretion inhibitor. Inhibin has been shown to regulate gonadal stromal cell proliferation negatively and to have tumor-suppressor activity. In addition, serum levels of inhibin have been shown to reflect the size of granulosa-cell tumors and can therefore be used as a marker for primary as well as recurrent disease. P08476 NM_002192 NP_002183.1

INHBA Antibody, EDF Antibody, Activin beta-A chain Antibody, FSH-releasing protein Antibody, Inhibin, beta A Antibody, Inhibin beta A chain Antibody, FRP Antibody, Inhibin Beta A Antibody, Inhibin, beta-1 Antibody


Specifications

Target
Human INHBA / Inhibin Beta A
Host
Rabbit
Reactivity
Human (tested or 100% immunogen sequence identity)
Predicted
Mouse, Rat, Cow (at least 90% immunogen sequence identity)
Clonality
Polyclonal
Conjugations
Unconjugated
Purification
Protein A purified
Modifications
Unmodified
Applications
  • IHC
  • IHC - Paraffin (1:10 - 1:50)
  • Immunofluorescence (1:10 - 1:50)
  • Western blot (1:1000)
  • Flow Cytometry (1:10 - 1:50)
Performing IHC? See our complete line of Immunohistochemistry Reagents including antigen retrieval solutions, blocking agents ABC Detection Kits and polymers, biotinylated secondary antibodies, substrates and more.
Blocking Peptide
LS-E772 - Lyophilized - 100 µg - $145.00
Immunizing peptide used to generate LS-C165241. Useful for pre-absorption and neutralization of the antibody's antigen binding site.
Epitope
aa85-112
Specificity
This INHBA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 85-112 amino acids from the N-terminal region of human INHBA.
Presentation
PBS, 0.09% sodium azide
Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
Restrictions
For research use only.
Guarantee
This antibody carries the LSBio 100% Guarantee.

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Images


Immunohistochemistry

INHBA Antibody immunohistochemistry of formalin-fixed and paraffin-embedded human stomach tissue followed by peroxidase-conjugated secondary antibody and DAB staining.
INHBA Antibody immunohistochemistry of formalin-fixed and paraffin-embedded human stomach tissue followed by peroxidase-conjugated secondary antibody and DAB staining.

Immunofluorescence

Confocal immunofluorescence of INHBA Antibody with HepG2 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).
Confocal immunofluorescence of INHBA Antibody with HepG2 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).

Western blot

INHBA Antibody western blot of CEM cell line lysates (35 ug/lane). The INHBA antibody detected the INHBA protein (arrow).
INHBA Antibody western blot of CEM cell line lysates (35 ug/lane). The INHBA antibody detected the INHBA protein (arrow).

Flow Cytometry

INHBA Antibody flow cytometry of CEM cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
INHBA Antibody flow cytometry of CEM cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Immunohistochemistry

INHBA Antibody immunohistochemistry of formalin-fixed and paraffin-embedded human stomach tissue followed by peroxidase-conjugated secondary antibody and DAB staining.
INHBA Antibody immunohistochemistry of formalin-fixed and paraffin-embedded human stomach tissue followed by peroxidase-conjugated secondary antibody and DAB staining.

Immunofluorescence

Confocal immunofluorescence of INHBA Antibody with HepG2 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).
Confocal immunofluorescence of INHBA Antibody with HepG2 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).

Western blot

INHBA Antibody western blot of CEM cell line lysates (35 ug/lane). The INHBA antibody detected the INHBA protein (arrow).
INHBA Antibody western blot of CEM cell line lysates (35 ug/lane). The INHBA antibody detected the INHBA protein (arrow).

Flow Cytometry

INHBA Antibody flow cytometry of CEM cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
INHBA Antibody flow cytometry of CEM cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Immunohistochemistry

INHBA Antibody immunohistochemistry of formalin-fixed and paraffin-embedded human stomach tissue followed by peroxidase-conjugated secondary antibody and DAB staining.
INHBA Antibody immunohistochemistry of formalin-fixed and paraffin-embedded human stomach tissue followed by peroxidase-conjugated secondary antibody and DAB staining.

Immunofluorescence

Confocal immunofluorescence of INHBA Antibody with HepG2 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).
Confocal immunofluorescence of INHBA Antibody with HepG2 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).

Western blot

INHBA Antibody western blot of CEM cell line lysates (35 ug/lane). The INHBA antibody detected the INHBA protein (arrow).
INHBA Antibody western blot of CEM cell line lysates (35 ug/lane). The INHBA antibody detected the INHBA protein (arrow).

Flow Cytometry

INHBA Antibody flow cytometry of CEM cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
INHBA Antibody flow cytometry of CEM cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Immunohistochemistry

INHBA Antibody immunohistochemistry of formalin-fixed and paraffin-embedded human stomach tissue followed by peroxidase-conjugated secondary antibody and DAB staining.
INHBA Antibody immunohistochemistry of formalin-fixed and paraffin-embedded human stomach tissue followed by peroxidase-conjugated secondary antibody and DAB staining.

Immunofluorescence

Confocal immunofluorescence of INHBA Antibody with HepG2 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).
Confocal immunofluorescence of INHBA Antibody with HepG2 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).

Western blot

INHBA Antibody western blot of CEM cell line lysates (35 ug/lane). The INHBA antibody detected the INHBA protein (arrow).
INHBA Antibody western blot of CEM cell line lysates (35 ug/lane). The INHBA antibody detected the INHBA protein (arrow).

Flow Cytometry

INHBA Antibody flow cytometry of CEM cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
INHBA Antibody flow cytometry of CEM cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.


Requested From: 
Date Requested: 6/23/2018

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