ARG62780

anti-CD235a antibody [HIR2]

anti-CD235a antibody [HIR2] for Agglutination,CyTOF®-candidate,Flow cytometry,IHC-Frozen sections,IHC-Formalin-fixed paraffin-embedded sections and Human

Cell Biology and Cellular Response antibody

Overview

Product Description Mouse Monoclonal antibody [HIR2] recognizes CD235a
Tested Reactivity Hu
Tested Application Agg, CyTOF®-candidate, FACS, IHC-Fr, IHC-P
Specificity The clone HIR2 recognizes N-terminal portion of glycophorin A (and weakly of glycophorin B). Its antigen is expressed on early erythroblasts, late erythroblasts, erythroblasts, mature erythrocytes and the cells of erythroid cell lines K562 and HEL, but not on all other cells.
HLDA VII; WS Code 70299
Host Mouse
Clonality Monoclonal
Clone HIR2
Isotype IgG2b
Target Name CD235a
Antigen Species Human
Immunogen Synthetic peptide (Human, N-terminal)
Conjugation Un-conjugated
Alternate Names MN; GPErik; MNS; GPA; GPSAT; PAS-2; MN sialoglycoprotein; CD235a; HGpMiV; CD antigen CD235a; HGpMiXI; Sialoglycoprotein alpha; HGpSta(C); Glycophorin-A

Application Instructions

Application Suggestion
Tested Application Dilution
AggAssay-dependent
CyTOF®-candidateAssay-dependent
FACS1 - 4 µg/ml
IHC-FrAssay-dependent
IHC-P10 µg/ml
Application Note Flow Cytometry: This HIR2 antibody has been tested by flow cytometric analysis of human peripheral blood leukocytes and cell agglutination assay and can be used at approximately 0.1 μg per million cells.
Agglutination: The antibody HIR2 agglutinates untreated RBCs but failes to agglutinate papain-treated cells.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purified by protein A
Purity > 95% (by SDS-PAGE)
Buffer PBS (pH 7.4) and 15 mM Sodium azide
Preservative 15 mM Sodium azide
Concentration 1 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 2993 Human GYPA

Swiss-port # P02724 Human Glycophorin-A

Gene Symbol GYPA
Gene Full Name glycophorin A (MNS blood group)
Background CD235a (Glycophorin A, GPA) is a transmembrane sialoglycoprotein expressed on erythrocytes and their precursors. Similarly to glycophorin B (GPB), these molecules provide the cells with a large mucin-like surface, which minimalizes aggregation between erythrocytes in the circulation. GPA is the carrier of blood group M and N specificities, while GPB accounts for S, s and U specificities. CD235a is a receptor of Hsa, an Streptococcus adhesin.
Function Glycophorin A is the major intrinsic membrane protein of the erythrocyte. The N-terminal glycosylated segment, which lies outside the erythrocyte membrane, has MN blood group receptors. Appears to be important for the function of SLC4A1 and is required for high activity of SLC4A1. May be involved in translocation of SLC4A1 to the plasma membrane. Is a receptor for influenza virus. Is a receptor for Plasmodium falciparum erythrocyte-binding antigen 175 (EBA-175); binding of EBA-175 is dependent on sialic acid residues of the O-linked glycans. Appears to be a receptor for Hepatitis A virus (HAV). [UniProt]
Highlight Related products:
CD235a antibodies; Anti-Mouse IgG secondary antibodies;
Related news:
CyTOF-candidate Antibodies
Research Area Cell Biology and Cellular Response antibody
Calculated MW 16 kDa
PTM The major O-linked glycan are NeuAc-alpha-(2-3)-Gal-beta-(1-3)-[NeuAc-alpha-(2-6)]-GalNAcOH (about 78 %) and NeuAc-alpha-(2-3)-Gal-beta-(1-3)-GalNAcOH (17 %). Minor O-glycans (5 %) include NeuAc-alpha-(2-3)-Gal-beta-(1-3)-[NeuAc-alpha-(2-6)]-GalNAcOH NeuAc-alpha-(2-8)-NeuAc-alpha-(2-3)-Gal-beta-(1-3)-GalNAcOH. About 1% of all O-linked glycans carry blood group A, B and H determinants. They derive from a type-2 precursor core structure, Gal-beta-(1,3)-GlcNAc-beta-1-R, and the antigens are synthesized by addition of fucose (H antigen-specific) and then N-acetylgalactosamine (A antigen-specific) or galactose (B antigen-specific). Specifically O-linked-glycans are NeuAc-alpha-(2-3)-Gal-beta-(1-3)-GalNAcOH-(6-1)-GlcNAc-beta-(4-1)-[Fuc-alpha-(1-2)]-Gal-beta-(3-1)-GalNAc-alpha (about 1%, B antigen-specific) and NeuAc-alpha-(2-3)-Gal-beta-(1-3)-GalNAcOH-(6-1)-GlcNAc-beta-(4-1)-[Fuc-alpha-(1-2)]-Gal-beta (1 %, O antigen-, A antigen- and B antigen-specific).

Images (2) Click the Picture to Zoom In

  • ARG62780 anti-CD235a antibody [HIR2] IHC-P image

    Immunohistochemistry: Paraffin-embedded Human adrenal tissue stained with ARG62780 anti-CD235a antibody [HIR2] at 10 µg/ml dilution.

  • ARG62780 anti-CD235a antibody [HIR2] FACS image

    Flow Cytometry: Human peripheral blood stained with ARG62780 anti-CD235a antibody [HIR2], followed by incubation with APC labelled Goat anti-Mouse secondary antibody.

Clone References

Proteomic analysis of ERK1/2-mediated human sickle red blood cell membrane protein phosphorylation.

WB, IP / Human

Soderblom EJ et al.
Clin Proteomics.,  (2013)

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Terminal differentiation and loss of tumorigenicity of human cancers via pluripotency-based reprogramming.

Zhang X et al.
Oncogene.,  (2013)

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A novel fluorescence-based method in forensic science for the detection of blood in situ.

ICC/IF / Human

Thorogate R et al.
Forensic Sci Int Genet.,  (2008)

publication_link

 

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[Immunophenotyping study on the blood cells of the patients with paroxysmal nocturnal hemoglobinuria].

Chen G et al.
Zhonghua Xue Ye Xue Za Zhi.,  (1997)

publication_link

 

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Flow cytometric analysis of human bone marrow perfusion cultures: erythroid development and relationship with burst-forming units-erythroid.

Rogers CE et al.
Exp Hematol.,  (1996)

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