Anticorps Polyclonal de lapin anti-SYNGAP1

SYNGAP1 Polyclonal Antibody for WB, IHC, IF/ICC, IP, Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain, porc, rat, souris

Applications

WB, IHC, IF/ICC, IP, Indirect ELISA

Conjugaison

Non conjugué

N° de cat : 19739-1-PBS

Synonymes

Neuronal RasGAP, Ras GTPase activating protein SynGAP, Ras/Rap GTPase-activating protein SynGAP, RASA 1, Synaptic Ras GTPase-activating protein 1

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Galerie de données de validation

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  WB analysis using 19739-1-AP (same clone as 19739-1-PBS)

  Various lysates were subjected to SDS PAGE followed by western blot with 19739-1-AP (SYNGAP1 antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 19739-1-PBS in a different storage buffer formulation.

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  WB analysis of mouse brain using 19739-1-AP (same clone as 19739-1-PBS)

  mouse brain tissue were subjected to SDS PAGE followed by western blot with 19739-1-AP (SYNGAP1 Antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 19739-1-PBS in a different storage buffer formulation.

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  IP experiment of mouse brain using 19739-1-AP (same clone as 19739-1-PBS)

  IP result of anti-SYNGAP1 (IP:19739-1-AP, 4ug; Detection:19739-1-AP 1:1500) with mouse brain tissue lysate 2120 ug. This data was developed using the same antibody clone with 19739-1-PBS in a different storage buffer formulation.

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  IHC staining of mouse brain using 19739-1-AP (same clone as 19739-1-PBS)

  Immunohistochemical analysis of paraffin-embedded mouse brain tissue slide using 19739-1-AP (SYNGAP1 Antibody) at dilution of 1:200 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 19739-1-PBS in a different storage buffer formulation.

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  IHC staining of mouse brain using 19739-1-AP (same clone as 19739-1-PBS)

  Immunohistochemical analysis of paraffin-embedded mouse brain tissue slide using 19739-1-AP (SYNGAP1 Antibody) at dilution of 1:200 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 19739-1-PBS in a different storage buffer formulation.

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  IF Staining of U-251 using 19739-1-AP (same clone as 19739-1-PBS)

  Immunofluorescent analysis of (-20°C Ethanol) fixed U-251 cells using SYNGAP1 antibody (19739-1-AP) at dilution of 1:200 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2). This data was developed using the same antibody clone with 19739-1-PBS in a different storage buffer formulation.

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Informations sur le produit

19739-1-PBS cible SYNGAP1 dans les applications de WB, IHC, IF/ICC, IP, Indirect ELISA et montre une réactivité avec des échantillons Humain, porc, rat, souris

• Réactivité: Humain, porc, rat, souris
• Hôte / Isotype: Lapin / IgG
• Clonalité: Polyclonal
• Type: Anticorps
• Immunogène: Peptide
• Nom complet: synaptic Ras GTPase activating protein 1 homolog (rat)
• Masse moléculaire calculée: 1343 aa, 148 kDa
• Poids moléculaire observé: 148 kDa
• Numéro d’acquisition GenBank: NM_006772
• Symbole du gène: SYNGAP1
• Identification du gène (NCBI): 8831
• Conjugaison: Non conjugué
• Forme: Liquide
• Méthode de purification: Purification par affinité contre l'antigène
• Tampon de stockage: PBS only
• Conditions de stockage: Store at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

SYNGAP1, also named as KIAA1938, is the major constituent of the PSD essential for postsynaptic signaling. It's an inhibitory regulator of the Ras-cAMP pathway. SYNGAP1 is a member of the NMDAR signaling complex in excitatory synapses, it may play a role in NMDAR-dependent control of AMPAR potentiation, AMPAR membrane trafficking and synaptic plasticity. SYNGAP1 regulates AMPAR-mediated miniature excitatory postsynaptic currents. SYNGAP1 may be involved in certain forms of brain injury, leading to long-term learning and memory deficits Defects in SYNGAP1 are the cause of mental retardation autosomal dominant type 5 (MRD5).

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