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AB134416

APC Anti-CD163 antibody [GHI/61]

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(5 Publications)

Mouse Monoclonal CD163 antibody - conjugated to APC. Suitable for Flow Cyt and reacts with Human samples. Cited in 5 publications. Immunogen corresponding to Cell preparation containing CD163 protein.

View Alternative Names

CD163, M130, Scavenger receptor cysteine-rich type 1 protein M130, Hemoglobin scavenger receptor

1 Images
Flow Cytometry - APC Anti-CD163 antibody [GHI/61] (AB134416)
  • Flow Cyt

Supplier Data

Flow Cytometry - APC Anti-CD163 antibody [GHI/61] (AB134416)

Surface staining of human peripheral blood using ab134416 at a dilution of 10 μL/100 μL. CD163 was detected on CD14+ monocytes, whereas CD14- lymphocytes were used as a negative control.

  • 578 PE

    PE Anti-CD163 antibody [GHI/61]

  • 578 PE

    PE Anti-CD163 antibody [GHI/61]

  • 695 PerCP/Cy5.5®

    PerCP/Cy5.5® Anti-CD163 antibody [GHI/61]

  • 387 mFluor™ UV375

    mFluor™ UV375 Anti-CD163 antibody [GHI/61]

  • 454 mFluor™ Violet 450

    mFluor™ Violet 450 Anti-CD163 antibody [GHI/61]

Key facts

Host species

Mouse

Clonality

Monoclonal

Clone number

GHI/61

Isotype

IgG1

Conjugation

APC

Excitation/Emission

Ex: 650nm, Em: 660nm

Carrier free

No

Reacts with

Human

Applications

Flow Cyt

applications

Immunogen

Cell preparation containing CD163 protein. The exact immunogen used to generate this antibody is proprietary information.

Q86VB7

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "FlowCyt" : {"fullname" : "Flow Cytometry", "shortname":"Flow Cyt"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "FlowCyt-species-checked": "testedAndGuaranteed", "FlowCyt-species-dilution-info": "10 µL for 10^6 Cells", "FlowCyt-species-notes": "<p>10 μl reagent / 100 μl of whole blood or 10<sup>6</sup> cells in a suspension.</p><p><a href='/en-us/products/primary-antibodies/apc-mouse-fab2-igg1-kappa-monoclonal-15h6-isotype-control-ab37391'>ab37391</a> - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody.</p>" } } }

Properties and storage information

Form
Liquid
Purification technique
Size-exclusion chromatography
Purification notes
Purity >95% by SDS-PAGE.
Storage buffer
pH: 7.4 Preservative: 0.1% Sodium azide Constituents: PBS, 0.2% BSA
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

CD163 known also as hemoglobin scavenger receptor is a membrane glycoprotein with a molecular weight of approximately 130 kDa. It is predominantly expressed by monocytes and macrophages which are types of immune cells. Located on the cell surface CD163 functions as a receptor that aids in the clearance of hemoglobin-haptoglobin complexes playing a critical role in maintaining iron homeostasis and protecting tissues from oxidative damage. CD163 is not limited to human cells only; researchers often study its function using animal models such as chimeric rodents and chimeric rats.
Biological function summary

CD163 participates in anti-inflammatory processes and is linked to immune modulation. It plays a pivotal role in the resolution of inflammation and promotes the removal of damaged cells and tissues. Through its involvement in the endocytic pathway CD163 interacts with various ligands facilitating interactions with other proteins. In the context of research CD163 functionality can be analyzed using techniques like CD163 IHC CD163 ELISA and CD163 stain in both human and mouse models.

Pathways

CD163 is integral to the inflammation and immune response pathways. It participates in the heme-oxygenase pathway which is essential in the breakdown of heme into biliverdin free iron and carbon monoxide. This pathway involvement is tightly linked with heme oxygenase-1 (HO-1) a cytoprotective enzyme that helps to mitigate inflammatory responses. The interaction with haptoglobin and related proteins provides further insight into its regulatory roles within the immune system.

CD163 is associated with conditions like atherosclerosis and acute inflammation disorders. Its elevated levels indicate macrophage activation observed in chronic inflammations such as cardiovascular diseases. In atherosclerosis CD163 expression correlates with the uptake of oxidized LDL connecting it to progression of the disease. Additionally soluble CD163 levels serve as a biomarker in conditions like chronic liver disease where it is linked to macrophage activation and fibrosis. Within these disorders proteins like LDL and inflammatory cytokines are closely associated with CD163 function and regulation.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Acute phase-regulated receptor involved in clearance and endocytosis of hemoglobin/haptoglobin complexes by macrophages and may thereby protect tissues from free hemoglobin-mediated oxidative damage. May play a role in the uptake and recycling of iron, via endocytosis of hemoglobin/haptoglobin and subsequent breakdown of heme. Binds hemoglobin/haptoglobin complexes in a calcium-dependent and pH-dependent manner. Exhibits a higher affinity for complexes of hemoglobin and multimeric haptoglobin of HP*1F phenotype than for complexes of hemoglobin and dimeric haptoglobin of HP*1S phenotype. Induces a cascade of intracellular signals that involves tyrosine kinase-dependent calcium mobilization, inositol triphosphate production and secretion of IL6 and CSF1. Isoform 3 exhibits the higher capacity for ligand endocytosis and the more pronounced surface expression when expressed in cells.. After shedding, the soluble form (sCD163) may play an anti-inflammatory role, and may be a valuable diagnostic parameter for monitoring macrophage activation in inflammatory conditions.
See full target information CD163

Publications (5)

Recent publications for all applications. Explore the full list and refine your search

Scientific reports 15:20507 PubMed40592997

2025

Sphingosine 1-phosphate derived from tumor-educated hepatic stellate cells combining with S1PR4 promotes tumor associated macrophages differentiation through FAO modulation.

Applications

Unspecified application

Species

Unspecified reactive species

Rui Feng,Zilin Cui,Long Yang,Zirong Liu

Journal of ovarian research 17:101 PubMed38745186

2024

Shikonin reduces M2 macrophage population in ovarian cancer by repressing exosome production and the exosomal galectin 3-mediated β-catenin activation.

Applications

Unspecified application

Species

Unspecified reactive species

Min Wang,Yangyan Sun,Rui Gu,Yan Tang,Guorong Han,Shaojie Zhao

Journal of cellular physiology 237:3627-3639 PubMed35766589

2022

Paracrine effect of the stromal vascular fraction containing M2 macrophages on human chondrocytes through the Smad2/3 signaling pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Masahiro Fujita,Tomoyuki Matsumoto,Shinya Hayashi,Shingo Hashimoto,Naoki Nakano,Toshihisa Maeda,Yuichi Kuroda,Yoshinori Takashima,Kenichi Kikuchi,Kensuke Anjiki,Kemmei Ikuta,Yuma Onoi,Shotaro Tachibana,Takehiko Matsushita,Hideki Iwaguro,Satoshi Sobajima,Takafumi Hiranaka,Ryosuke Kuroda

Cell death & disease 10:918 PubMed31801938

2019

Gastric cancer-derived mesenchymal stromal cells trigger M2 macrophage polarization that promotes metastasis and EMT in gastric cancer.

Applications

Unspecified application

Species

Unspecified reactive species

Wei Li,Xu Zhang,Fenglei Wu,Ying Zhou,Zengtao Bao,Haining Li,Ping Zheng,Shaolin Zhao

Biomaterials 35:4477-88 PubMed24589361

2014

The role of macrophage phenotype in vascularization of tissue engineering scaffolds.

Applications

Unspecified application

Species

Unspecified reactive species

Kara L Spiller,Rachel R Anfang,Krista J Spiller,Johnathan Ng,Kenneth R Nakazawa,Jeffrey W Daulton,Gordana Vunjak-Novakovic
View all publications

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