• Product name
  • Description
    Goat polyclonal to CCR8
  • Host species
  • Specificity
    Peptide sequence is < 50 % identical to other human chemokine receptors in this region.
  • Tested applications
    Suitable for: WB, ELISA, Flow Cyt, ICC, IHC-Pmore details
  • Species reactivity
    Reacts with: Human
  • Immunogen

    Synthetic peptide:


    , corresponding to amino acids 12-36 of Human CCR8.

  • Positive control
    • Human K562 cells or tissue sections of spleen.



Our Abpromise guarantee covers the use of ab1666 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 1/2000.
ELISA 1/100000.
Flow Cyt Use 1-3µl for 106 cells.

ab37373 - Goat polyclonal IgG, is suitable for use as an isotype control with this antibody.


ICC 1/800.
IHC-P 1/250.


  • Function
    Receptor for the chemokine CCL1/SCYA1/I-309. May regulate monocyte chemotaxis and thymic cell line apoptosis. Alternative coreceptor with CD4 for HIV-1 infection.
  • Sequence similarities
    Belongs to the G-protein coupled receptor 1 family.
  • Cellular localization
    Cell membrane.
  • Information by UniProt
  • Database links
  • Alternative names
    • C C chemokine receptor type 8 antibody
    • C C CKR 8 antibody
    • C C motif chemokine receptor 8 antibody
    • C-C chemokine receptor type 8 antibody
    • C-C CKR-8 antibody
    • CC chemokine receptor 8 antibody
    • CC chemokine receptor CHEMR1 antibody
    • CC chemokine receptor type 8 antibody
    • CC CKR 8 antibody
    • CC-CKR-8 antibody
    • CCR 8 antibody
    • CCR-8 antibody
    • Ccr8 antibody
    • CCR8 protein antibody
    • CCR8-L antibody
    • CCR8_HUMAN antibody
    • CDw198 antibody
    • CDw198 antigen antibody
    • Chemokine (C C motif) receptor 8 antibody
    • Chemokine (C C) receptor 8 antibody
    • Chemokine (C C) receptor like 2 antibody
    • Chemokine (CC motif) receptor 8 antibody
    • Chemokine (CC) receptor 8 antibody
    • Chemokine (CC) receptor like 1 antibody
    • Chemokine (CC) receptor like 2 antibody
    • Chemokine C C motif receptor 8 antibody
    • Chemokine C C receptor 8 antibody
    • Chemokine CC motif receptor 8 antibody
    • Chemokine CC receptor 8 antibody
    • Chemokine receptor 8 antibody
    • Chemokine receptor like 1 antibody
    • Chemokine receptor-like 1 antibody
    • CKR L1 antibody
    • CKR-L1 antibody
    • CKRL 1 antibody
    • CKRL1 antibody
    • CMKBR 8 antibody
    • CMKBR L2 antibody
    • CMKBR8 antibody
    • CMKBRL 2 antibody
    • CMKBRL2 antibody
    • CY 6 antibody
    • CY6 antibody
    • GPR CY6 antibody
    • GPR-CY6 antibody
    • GPRCY6 antibody
    • MGC123958 antibody
    • MGC123959 antibody
    • MGC129966 antibody
    • MGC129973 antibody
    • TER 1 antibody
    • TER1 antibody
    see all


  • Immunohistochemistry using ab1666 on a paraffin section of human spleen. 


ab1666 has not yet been referenced specifically in any publications.

Customer reviews and Q&As

1-2 of 2 Abreviews or Q&A


Thank you for your response.

I agree that it is imperative to be able to determine whether there is more or less of this protein expressed in your samples. To determine this I think we need to be able to exclude the possibility that there are other issues, not related to the antibodies, which are affecting this. In the proposal that I have outlined you will be able to directly compare the over expressed, knockdown and endogenous levels simultaneously with differing total protein concentrations. This way we will be able to say conclusively whether or not the antibody is detecting the different levels.

Unfortunately we do not have sample size aliquots of our products. The antibody is covered under our Abpromise for six months and is guaranteed to work in WB on human samples. If you are experiencing issues with this product and we cannot resolve the issue you are having, then I would be happy to either send a replacement antibody or to process a refund.

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Thank you for sending me this data, it has been very useful in understanding the issues that you are facing.

I would suggest performing a set of experiments were you load an increasing amount of your sample in wells. For example, load 5 wells with 5ug, 15ug, 25ug, 50ug and 100ug of your untreated sample. Run these in conjunction with similar amounts of your shRNA and siRNA treated lines and compare the results.

I hope that this information is helpful. Please let me know your results and do not hesitate to let me know if you have any questions or there are other ways that Abcam may help you meet your research goals.

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