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Semaphorin 3A Antibody (2701F) [Unconjugated]

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Semaphorin 3A was detected in immersion fixed C2C12 mouse myoblast cell line (positive staining) and K562 human chronic myelogenous leukemia cell line (negative staining) using Rabbit Anti-Mouse Semaphorin 3A ...read more

Product Details

Summary
Reactivity MuSpecies Glossary
Applications ICC/IF
Clone
2701F
Clonality
Monoclonal
Host
Rabbit
Conjugate
Unconjugated

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Semaphorin 3A Antibody (2701F) [Unconjugated] Summary

Additional Information
Recombinant Monoclonal Antibody.
Immunogen
Chinese Hamster Ovary cell line, CHO-derived mouse SEMA 3A
Asn21-Lys747
Accession # O08665
Specificity
Detects mouse SEMA 3A
Source
N/A
Isotype
IgG
Clonality
Monoclonal
Host
Rabbit
Purity Statement
Protein A or G purified from cell culture supernatant
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Immunocytochemistry 3-25 ug/mL

Packaging, Storage & Formulations

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.
Buffer
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.
Reconstitution Instructions
Reconstitute at 0.5 mg/mL in sterile PBS.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Semaphorin 3A Antibody (2701F) [Unconjugated]

  • (semaphorin) 3A
  • coll-1
  • collapsin 1
  • Hsema-I
  • Hsema-III
  • MGC133243
  • sema domain, immunoglobulin domain (Ig), short basic domain, secreted
  • Sema III
  • SEMA1
  • Sema3A
  • SEMAD
  • SEMAIII
  • SEMAL
  • Semaphorin 3A
  • semaphorin D
  • Semaphorin III
  • semaphorin L
  • semaphorin-3A
  • SemD

Background

Semaphorin 3A (Sema3A; previously sem D, sema III or collapsin) is one of six Class 3 secreted semaphorins which share ~40-50% amino acid (aa) identity
(1-3). Class 3 semaphorins are potent chemorepellents that function in axon and/or vascular guidance during development (2, 3). The 772 aa mouse Sema3C contains a 20 aa signal sequence, an ~500 aa N-terminal Sema domain that forms a beta -propeller structure similar to that found in integrin molecules, a PSI domain, a furin-type cleavage site, an Ig-like domain, and a C-terminal basic domain (3, 4). Covalent dimerization plus cleavage at the C-terminus are required for activity of class 3 semaphorins (5, 6). The 95 kDa mature mouse Sema3A shares at least 95% aa identity with human, rat, equine and canine Sema3A, and 90% and 86% aa identity with chick and zebrafish Sema3A, respectively. Type 3 semaphorins transduce signals through transmembrane plexins, either directly or by binding associated neuropilin receptors (3). Sema3A signaling is transduced by plexin A1-4, indirectly via neuropilin-1 (3). Sema3A activity is mediated by small GTPases that influence actin rearrangement and integrin activity (7-9). It is important in developmental organization of central and peripheral nerves, including those in heart, lung, kidneys, bones, teeth, and visual and olfactory systems (1, 2, 10, 11). Gradients of Sema3A repel axons, but attract dendrites (11, 12). Sema3A affect vasculogenesis by inhibiting integrin function and, with Sema3F, promoting apoptosis of endothelial cells (3, 9, 12). It is thought to suppress cancer-related angiogenesis (3). In the immune system, Sema3A influences T cell proliferation, migration, response to activation, and interactions with dendritic cells (7, 13). It negatively regulates platelet activation (14). Expression of Sema3A in relevant parts of the nervous system may be increased in Alzheimer’s disease, multiple sclerosis, ischemia and schizophrenia (2).

  1. Puschel, A.W. et al. (1995) Neuron 14:941.
  2. Roth, L. et al. (2009) Cell. Mol. Life Sci. 66:649.
  3. Neufeld, G and O. Kessler (2008) Nat. Rev. Cancer 8:632.
  4. Gherardi, E. et al. (2004) Curr. Opin. Struct. Biol. 14:669.
  5. Adams, R. H. et al. (1997) EMBO J. 16:6077.
  6. Klosterman, A. et al. (1998) J. Biol. Sci. 273:7326.
  7. Lepelletier, Y. et al. (2006) Eur. J. Immunol. 36:1782.
  8. Schlomann, U. et al. (2009) J. Cell Sci. 122:2034.
  9. Serini, G. et al. (2003) Nature 424:391.
  10. Ieda, M. et al. (2007) Nat. Med. 13:604.
  11. Chen, G. et al. (2008) Nat. Neurosci. 11:36.
  12. Guttmann-Raviv, N. et al. (2007) J. Biol Chem. 282:26294.
  13. Lepelletier, Y. et al. (2007) Proc. Natl. Acad. Sci. USA 104:5545.
  14. Kashiwagi, H. et al. (2005) Blood 106:913.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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