• Product name

    Anti-AMHR2 antibody - Aminoterminal end
    See all AMHR2 primary antibodies
  • Description

    Rabbit polyclonal to AMHR2 - Aminoterminal end
  • Host species

  • Tested applications

    Suitable for: WB, ELISA, ICC/IFmore details
  • Species reactivity

    Reacts with: Human
  • Immunogen

    KLH conjugated synthetic peptide selected from the N terminal region of human AMHR2.

  • Positive control

    • Transfected 293 cell lysates. This antibody gave a positive result when used in the following formaldehyde fixed cell lines: A549



Our Abpromise guarantee covers the use of ab75845 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB 1/50 - 1/100. Predicted molecular weight: 63 kDa.
ELISA 1/1000.
ICC/IF Use a concentration of 5 µg/ml.


  • Function

    On ligand binding, forms a receptor complex consisting of two type II and two type I transmembrane serine/threonine kinases. Type II receptors phosphorylate and activate type I receptors which autophosphorylate, then bind and activate SMAD transcriptional regulators. Receptor for anti-Muellerian hormone.
  • Involvement in disease

    Defects in AMHR2 are the cause of persistent Muellerian duct syndrome type 2 (PMDS2) [MIM:261550]. PMDS2 is a form of male pseudohermaphroditism characterized by a failure of Muellerian duct regression in otherwise normal males.
  • Sequence similarities

    Belongs to the protein kinase superfamily. TKL Ser/Thr protein kinase family. TGFB receptor subfamily.
    Contains 1 protein kinase domain.
  • Cellular localization

  • Information by UniProt
  • Database links

  • Alternative names

    • AMH type II receptor antibody
    • AMHR antibody
    • AMHR2 antibody
    • AMHR2_HUMAN antibody
    • Anti Mullerian hormone receptor, type II antibody
    • Anti-Muellerian hormone type II receptor antibody
    • Anti-Muellerian hormone type-2 receptor antibody
    • MGC141312 antibody
    • MIS type II receptor antibody
    • MISR2 antibody
    • MISRII antibody
    • MRII antibody
    • Muellerian hormone type 2 receptor antibody
    • Muellerian hormone type II receptor antibody
    • Muellerian inhibiting substance type II receptor antibody
    • Mullerian hormone receptor type II antibody
    • Mullerian inhibiting substance type II receptor antibody
    see all


  • ICC/IF image of ab75845 stained A549 cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody ab75845 at 5µg/ml overnight at +4°C. The secondary antibody (green) was DyLight® 488 goat anti- rabbit (ab96899) IgG (H+L) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.

  • All lanes : Anti-AMHR2 antibody - Aminoterminal end (ab75845) at 1/50 dilution

    Lane 1 : Non transfected 293 cell lysates
    Lane 2 : Transiently transfected 293 cell lysates

    Lysates/proteins at 2 µg per lane.

    Predicted band size: 63 kDa
    Observed band size: 63 kDa


ab75845 has not yet been referenced specifically in any publications.

Customer reviews and Q&As

1-3 of 3 Abreviews or Q&A


Thank you for contacting us.

Your credit note ID is XXXXXX

I am sorry that this antibody did not perform as stated on the datasheet, I have asked our Finance department to issue a credit note for you. The credit note may be used in one of the following ways:

(1) Redeemed against the original invoice if this hasn't already been paid.
(2) Held on the account for use against a future order.
(3) A full refund can be offered where no other invoices are outstanding.

Please contact your Finance department to confirm how you would like the credit note to be used and ensure it is not redeemed without your knowledge.

To specifically receive a refund please ask your Finance department to contact our Finance department at creditcontrol@abcam.com or by telephone using the information at the “Contact Us” link in the top right corner of our website.

The credit note ID is for your reference only, please refer to the credit note ID in any correspondence with our accounting department. We will send you the completed credit note by email or postal mail with the actual credit note number which will start with the letters CGB.

I hope this experience will not prevent you from purchasing other products from us in the future. Our Scientific Support team is always at your service should you require further expert advice

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Thanks you for your email. Dr. Tanya is away this week so I am dealing with her inquiries.
I am sorry that the product did not perform well. I can provide a free of charge replacement, refund or credit note. Could you please confirm how the customer would like to proceed?

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Dear technical support team:

This customer has purchased ab75845 (Anti-AMHR2 antibody - Aminoterminal end) and has conducted the wb several times with human sample. The results show wrong band size and more bands, therefore this customer wants to ask for your help to modify her experiment step, could you please offer any suggestion to improve her results? I attached the image in this letter and his experiment step as follow:

1. Order details:

Batch number: GR61389-1

Abcam product code: ab75845

Antibody storage conditions (temperature/reconstitution etc) : -20℃

2. Please describe the problem: wrong band size, and more bands!

3. On what material are you testing the antibody in WB?

· Species: Human

· What’s cell line or tissue : HCC cell line, Hep3B and ML

· Cell extract or Nuclear extract: Cell extract

· Purified protein or Recombinant protein: No

3. The lysate

How much protein was loaded: 15 ug

What lysis buffer was used: RIPA

What protease inhibitors were used: Na3VO4, EDTA, PMSF, NaF

What loading buffer was used: 4X loading buffer(with DTT)

Phosphatase inhibitors : Na3VO4, NaF

Did you heat the samples: temperature and time: 95℃,5 mins

4. Electrophoresis/Gel conditions/ Transfer conditions

Reducing or non reducing gel: reducing gel

Reducing agent: DTT

Gel percentage : 10%

Transfer conditions: (Type of membrane, Protein transfer verified): PVDF membrane, 5% methanol 1X Transfer buffer.

5. Blocking conditions

Buffer: 5% BSA(TBST)

Blocking agent: BSA

Incubation time: O/N

Incubation temperature:4 ℃

6. Primary Antibody

Species: Rabbit

Reacts against: Reacts with Human

· At what dilution(s) have you tested this antibody: 1:50

· What dilution buffer was used: 5% BSA(TBST)

· Incubation time: 2 hr

· Incubation temperature: RT (25℃)

· What washing steps were done: TBST wash three times,10 min each time

7. Secondary Antibody

Species: Gt X Rb IgG(H+L) HRP , 4℃, Millipore

Reacts against: Reacts with Rabbit

At what dilution(s) have you tested this antibody: 1/2000,5% milk

Incubation time: 50 mins

Wash steps: TBST wash three times,10 min each time

Fluorochrome or enzyme conjugate: enzyme conjugate

Do you know whether the problems you are experiencing come from the secondary? I sure it’s no problems.

8. Detection method
ECl, ECl+, other detection method:
Western HRP Substrate.WBKLS0500 - Millipore

9. Did you apply positive and negative controls along with the samples? Please specify. No

10. Optimization attempts

· How many times have you tried the Western? 3 times

· Have you eliminated the possibility that any background bands could be due to the secondary antibody? (Run a “No primary” control): No

· Do you obtain the same results every time e.g. are background bands always in the same place? Yes, the same results.

· What steps have you altered? Concentration of primary antibody

Could you please help this customer to solve the problem?

Thanks for your kindly help

Best regards

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Thank you for your enquiry regarding ab75845 and for taking the time to provide some useful details of the experiments. I am very sorry to hear that you are having problems with this antibody.

1) Transfection:

a) Could you please explain what these abbreviations represent provided on the Western blot image?

ML shControl,

ML shAMHR2 (G9),

ML shAMHR2 (B10),

3B transfection control,

3B siAMHR2 (s5),

3B siAMHR2 (s6)

b) Looking at the signal of the loading control it seems that not the same amount of protein was loaded onto the gel. Could you explain if the customer has performed any time-course experiments which may influence the expression of the actin. What is the sizeof the actin on the blot, could you please label the image with MW for the actin as well?

c) Does the construct contain full sequence or fragment of the target protein? Does it correspond to human AMHR2 sequences?

c) Could you please confirm if the target protein is tagged, if so which tag(s) was used?

c) How was the efficiency of the transfection checked?

2) Secondary antibody:

a) Does the detection system work fine? Have you used it successfully with another primary antibody?

b) Have you run a no primary - only secondary antibody - control to see if any of the non-specific bands are due to the secondary or not? If you have not done yet, I would advise you to check it.

Thank you for your understanding and co-operation in this matter. I look forward to hearing from you and hope to solve this problem as soon as possible.

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