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MABC184

Sigma-Aldrich

Anti-SDF-1 Antibody, clone K15C, Azide free

clone K15C, from mouse

Synonym(s):

Stromal cell-derived factor 1, SDF-1, hSDF-1, C-X-C motif chemokine 12, Intercrine reduced in hepatomas, IRH, hIRH, Pre-B cell growth-stimulating factor, PBSF

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

biological source

mouse

Quality Level

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

K15C, monoclonal

species reactivity

mouse, human

technique(s)

ELISA: suitable
immunohistochemistry: suitable
neutralization: suitable
western blot: suitable

isotype

IgG2aκ

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... CXCL12(6387)

General description

Stromal cell-derived factor 1 (SDF-1) is also known as C-X-C motif chemokine 12 (CXCL12), Intercrine reduced in hepatomas (IRH), and Pre-B cell growth-stimulating factor (PBSF). SDF-1 is a chemoattractant active on T-lymphocytes, monocytes, but not neutrophils. SDF-1 stimulates migration of monocytes and T-lymphocytes through its receptors, CXCR4 and CXCR7, and decreases monocyte adherence to surfaces coated with ICAM-1. SDF-1 plays a protective role after myocardial infarction, has critical functions during embryonic development and is required for B-cell lymphopoiesis, myelopoiesis in bone marrow and heart ventricular septum formation. Isoform Alpha and isoform Beta are ubiquitously expressed, with highest levels detected in liver, pancreas and spleen. Isoform Gamma is mainly expressed in heart. Isoform Delta, isoform Epsilon and isoform Theta have highest expression levels in pancreas.

Specificity

This antibody recognizes the N-terminus of SDF-1. This antibody should detected SDF-1alpha and SDF-1beta.

Immunogen

BSA-conjugated linear peptide corresponding to human SDF-1.
Epitope: N-terminus

Application

Detect SDF using this mouse monoclonal antibody, Anti-SDF-1 Antibody, clone K15C, Azide free validated for use in western blotting, IHC, Neutralizing & ELISA.
Research Category
Apoptosis & Cancer
Research Sub Category
Growth Factors & Receptors
Western Blotting Analysis: 0.375 µg/mL from a representative lot detected SDF-1 in 10 µg of HeLa and RAW264.7 cell lysates.

Western Blotting Analysis: A representative lot from an independent laboratory detected SDF-1alpha, SDF-1beta, and SDF-IP10 chimera, but not IP-10, IL-8, MDC, MIP-1b, eotaxin, and RANTES in WB (Coulomb-L′Hermin, A., et al. (1999). Proc Natl Acad Sci USA. 96(15):8585-8590.).

ELISA Analysis: A representative lot from an independent laboratory detected SDF-1alpha, SDF-1beta, and SDF-IP10 chimera, but not IP-10, IL-8, MDC, MIP-1b, eotaxin, and RANTES in ELISA (Coulomb-L′Hermin, A., et al. (1999). Proc Natl Acad Sci USA. 96(15):8585-8590.).

Immunohistochemistry Analysis: A representative lot from an independent laboratory detected SDF-1 in human fetal liver, lung, and kidney tissues (Coulomb-L′Hermin, A., et al. (1999). Proc Natl Acad Sci USA. 96(15):8585-8590.).

Neutralization Analysis: A representative lot from an independent laboratory attenuates the increased growth of MCF-7-ras tumor development in the presence of CAFs, decreases angiogenesis, and reduced recruitment of EPCs in tumors (Orimo, A., et al. (2005). Cell. 121(3):335-348.).

Immunhistochemistry Analysis: A representative lot from an independent laboratory detected SDF-1 in epidermal Dendritic Cells (DC) in normal and autoimmune diseased skin tissue (Pablos, J. L., et al. (1999). Am J Pathol. 155(5):1577-1586.).

Immunohistochemistry Analysis: A representative lot from an independent laboratory detected SDF-1 in mucosal surfaces of small intestine tissue, rectal tissue, vaginal tissue, and endocervical tissue (Agace, W. W., et al. (2000). Curr Biol. 10(6):325-328.).

Immunohistochemistry Analysis: A representative lot from an independent laboratory detected SDF-1 in mouse bone marrow sections (Dar, A., et al (2005). Nat Immunol. Epub 2005.).

Quality

Evaluated by Western Blotting in HEPG2 cell lysate.

Western Blotting Analysis: 0.375 µg/mL of this antibody detected SDF-1 in 10 µg of HEPG2 cell lysate.

Target description

~18 kDa observed. The calculated molecular weight of the SDF-1 monomer is 9 kDa However, the SDF-1 dimer has been observed at ~18 kDa (Veldkamp, C. T., et al. (2008). Sci Signal. 1(37):ra4.).

Physical form

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG2aκ in buffer containing PBS without preservatives.

Storage and Stability

Stable for 1 year at -20°C from date of receipt.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.

Analysis Note

Control
HEPG2 cell lysate

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Mitra J Hooshmand et al.
Journal of immunology (Baltimore, Md. : 1950), 199(3), 1069-1085 (2017-07-09)
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Influenza A virus (IAV) is recognized to cause severe pulmonary illnesses in humans, particularly in elderly and children. One of the features associated with IAV infection is an excessive lung inflammation due to an uncontrolled immune response. The nucleotide-binding oligomerization
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Glaucoma is the leading cause of irreversible vision loss, and reducing elevated intraocular pressure is currently the only effective clinical treatment. The trabecular meshwork is the main resistance site for aqueous outflow that maintains intraocular pressure. In this study, we
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PLoS neglected tropical diseases, 10(4), e0004605-e0004605 (2016-04-26)
Our knowledge and control of the pathogenesis induced by the filariae remain limited due to experimental obstacles presented by parasitic nematode biology and the lack of selective prophylactic or curative drugs. Here we thought to investigate the role of neutrophils
Juanli Qiao et al.
Oncotarget, 7(29), 46088-46099 (2016-06-22)
It has been suggested that the overexpression of serum response factor (SRF) in cancer cells may promote cancer metastasis. However, the exact pathway by which SRF promotes metastasis has not been clarified. Here we showed that SRF promotes gastric cancer

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