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Anti-Rapsyn antibody [1234] (ab11423)

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Overview

Product name

Anti-Rapsyn antibody [1234]
See all Rapsyn products (4) ...

Description

Mouse monoclonal [1234] to Rapsyn

Tested applications

WB, IF, ICC, IHC-Frmore details

Cross reactivity

Reacts with

Mouse, Rat, Chicken, Fish

Predicted to work with

Amphibians

Immunogen

Whole purified rapsyn from Torpedo californica electric organ postsynaptic membrane.

Positive control

Torpedo californica electrocyte cell extracts.

Properties

Form

Liquid

Storage instructions

Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

Storage buffer

Preservative: 0.05% Sodium Azide
Constituents: PBS, 1mg/ml BSA

Concentration

Concentration information loading...

Purity

Protein G purified

Clonality

Monoclonal

Clone number

1234

Isotype

IgG1

Applications

Show applications key

Our Abpromise guarantee covers the use of ab11423 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application notes

ICC: Use at an assay dependent dilution.
IF: Use at a concentration of 2 µg/ml.
IHC-Fr: Use at an assay dependent dilution.
WB: Use at a concentration of 0.5 µg/ml. Detects a band of approximately 48 kDa, representing rapsyn from Torpedo californica electrocyte cell extracts.

Not tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.

Target

Function

Thought to play some role in anchoring or stabilizing the nicotinic acetylcholine receptor at synaptic sites. It may link the receptor to the underlying postsynaptic cytoskeleton, possibly by direct association with actin or spectrin.

Involvement in disease

Defects in RAPSN are a cause of congenital myasthenic syndrome with acetylcholine receptor deficiency (ACHRDCMS) [MIM:608931]. ACHRDCMS is a post-synaptic congenital myasthenic syndrome. Congenital myasthenic syndromes (CMS) are inherited disorders of neuromuscular transmission that stem from mutations in presynaptic, synaptic, or postsynaptic proteins. Postsynaptic disorders result from mutations in proteins forming the subunits of the muscle acetylcholine receptor (AChR). The kinetic abnormalities of AChR result in either prolonged ion channel activations that underlie 'slow-channel myasthenic syndromes' (SCCMS) or abbreviated channel activations that underlie the abnormally rapid decay of endplate currents in 'fast-channel syndromes' (FCCMS). ACHRDCMS is the third disorder associated with postsynaptic CMS which could result from mutations in the proteins forming the muscle AChR. Mutations underlying AChR deficiency cause a 'loss of function' and show recessive inheritance.
Defects in RAPSN are the cause of fetal akinesia deformation sequence (FADS) [MIM:208150]; also known as Pena-Shokeir syndrome type 1 or fetal akinesia sequence or arthrogryposis multiplex congenita with pulmonary hypoplasia. FADS is a rare condition characterized by decreased intrauterine fetal movement, congenital limb contractures, pulmonary hypoplasia, polyhydramnios and craniofacial abnormalities.

Sequence similarities

Belongs to the RAPsyn family.
Contains 1 RING-type zinc finger.
Contains 7 TPR repeats.

Domain

A cysteine-rich region homologous to part of the regulatory domain of protein kinase C may be important in interactions of this protein with the lipid bilayer.

Cellular localization

Cell membrane. Cell junction > synapse > postsynaptic cell membrane. Cytoplasm > cytoskeleton. Cytoplasmic surface of postsynaptic membranes.

Target information above from: UniProt accessionQ13702 The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).

Information by UniProt

Alternative names

  • 43 kD receptor associated protein of the synapse antibody
  • 43 kda postsynaptic protein antibody
  • 43 kDa receptor-associated protein of the synapse antibody
  • Acetylcholine receptor associated 43 kda protein antibody
  • acetylcholine receptor-associated 43 kda protein antibody
  • CMS1D antibody
  • CMS1E antibody
  • MGC3597 antibody
  • RAPSN antibody
  • RAPSN_HUMAN antibody
  • RAPsyn antibody
  • Receptor associated protein of the synapse 43kD antibody
  • Receptor associated protein of the synapse antibody
  • receptor-associated protein of the synapse 43kD antibody
  • RING finger protein 205 antibody
  • RNF 205 antibody
  • RNF205 antibody
see all

References for Anti-Rapsyn antibody [1234] (ab11423)

This product has been referenced in:

  • Cossins Jet al. Diverse molecular mechanisms involved in AChR deficiency due to rapsyn mutations. Brain 129:2773-83 (2006).Read more (PubMed: 16945936) »
  • Stetzkowski-Marden Fet al. Agrin elicits membrane lipid condensation at sites of acetylcholine receptor clusters in C2C12 myotubes. J Lipid Res 47:2121-33 (2006).Read more (PubMed: 16816402) »

See all 2 publications for this product

Publishing research using ab11423? Please let us know so that we can cite the reference in this datasheet

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"