NM23-H2 or NME-2 (non-metastatic cell 2; also Nucleoside diphosphate kinase B, nm23-H2/B, NDPK-B and PUF) is a 17-19 kDa class 1 member of the NME/NDPK family of molecules. It is widely expressed, found in both cytosol and nucleus, and participates in multiple activities. In conjunction with nm23-H1, NME-2 forms homo- and heterohexamers (three dimers or two trimers) that mediate the transfer of phosphate from ATP to nucleoside diphosphates. It also serves as a transcriptional regulator of genes such as c-myc and PDGF-A. Human NME-2 is 152 amino acids (aa) in length. It contains a kinase region (aa 5-134), two potential phosphorylation sites (Tyr52 and Thr94), a phosphohistidine residue at position 118, and multiple lysine acetylation sites. There is one potential NME-2 splice form that shows a six aa substitution for aa 77-152. The genes for NME-1 and NME-2 are adjacent, and an unusual splicing event generates a 33 kDa fusion protein (NM23-LV) that is composed of aa 1-114 of NME-1 plus a Thr insert that is N-terminally coupled to full-length NME-2. Full-length human NME-2 shares 88% and 98% aa identity with human NME-1 and mouse NME-2, respectively.
Human NM23‑H2 Antibody
R&D Systems | Catalog # AF6665
Key Product Details
Species Reactivity
Validated:
Human
Cited:
Human
Applications
Validated:
Western Blot, Immunocytochemistry
Cited:
Western Blot, Immunocytochemistry
Label
Unconjugated
Antibody Source
Polyclonal Sheep IgG
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Product Specifications
Immunogen
E. coli-derived recombinant human NM23-H2
Ala2-Glu152
Accession # P22392
Ala2-Glu152
Accession # P22392
Specificity
Detects human NM23-H2 in direct ELISAs and Western blots. In direct ELISAs, less than 1% cross-reactivity with recombinant human NM23‑H1 is observed.
Clonality
Polyclonal
Host
Sheep
Isotype
IgG
Scientific Data Images for Human NM23‑H2 Antibody
Detection of Human NM23‑H2 by Western Blot.
Western blot shows lysates of Capan-1 human pancreatic adenocarcinoma cell line and MCF-7 human breast cancer cell line. PVDF Membrane was probed with 1 µg/mL of Sheep Anti-Human NM23-H2 Polyclonal Antibody (Catalog # AF6665) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # HAF016). Specific bands were detected for NM23-H2 at approximately 20 and 23 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 8.NM23‑H2 in MCF‑7 Human Cell Line.
NM23-H2 was detected in immersion fixed MCF-7 human breast cancer cell line using Sheep Anti-Human NM23-H2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF6665) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Sheep IgG Secondary Antibody (red; Catalog # NL010) and counterstained with DAPI (blue). Specific staining was localized to cytoplasm. View our protocol for Fluorescent ICC Staining of Cells on Coverslips.Applications for Human NM23‑H2 Antibody
Application
Recommended Usage
Immunocytochemistry
5-15 µg/mL
Sample: Immersion fixed MCF‑7 human breast cancer cell line
Sample: Immersion fixed MCF‑7 human breast cancer cell line
Western Blot
1 µg/mL
Sample: Capan‑1 human pancreatic adenocarcinoma cell line and MCF‑7 human breast cancer cell line
Sample: Capan‑1 human pancreatic adenocarcinoma cell line and MCF‑7 human breast cancer cell line
Formulation, Preparation, and Storage
Purification
Antigen Affinity-purified
Reconstitution
Sterile PBS to a final concentration of 0.2 mg/mL. For liquid material, refer to CoA for concentration.
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Formulation
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.
Shipping
Lyophilized product is shipped at ambient temperature. Liquid small pack size (-SP) is shipped with polar packs. Upon receipt, store immediately at the temperature recommended below.
Stability & Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: NM23-H2
Long Name
Non-metastatic Protein 23 Homolog 2
Alternate Names
NDK B, NDP Kinase B2, NDPKB, NM23B, NME2
Gene Symbol
NME2
UniProt
Additional NM23-H2 Products
Product Documents for Human NM23‑H2 Antibody
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Human NM23‑H2 Antibody
For research use only
Related Research Areas
Citations for Human NM23‑H2 Antibody
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars
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