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IQSEC2 Rabbit pAb
- 产品详情
- 实验流程
Application 
| IHC-P, IHC-F, IF |
|---|---|
| Primary Accession | Q5JU85 |
| Other Accession | Q5JU85 |
| Reactivity | Mouse |
| Predicted | Rat, Pig, Human, Dog, Sheep |
| Host | Rabbit |
| Clonality | Polyclonal |
| Calculated MW | 162784 Da |
| Physical State | Liquid |
| Immunogen | KLH conjugated synthetic peptide derived from human IQSEC2 |
| Epitope Specificity | 851-950/1478 |
| Isotype | IgG |
| Purity | affinity purified by Protein A |
| Buffer | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| SIMILARITY | Belongs to the BRAG family. Contains 1 IQ domain. Contains 1 PH domain. Contains 1 SEC7 domain. |
| DISEASE | Defects in IQSEC2 are the cause of mental retardation X-linked type 1 (MRX1) [MIM:309530]. Mental retardation is characterized by significantly below average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. In contrast to syndromic or specific X-linked mental retardation which also present with associated physical, neurological and/or psychiatric manifestations, intellectual deficiency is the only primary symptom of non-syndromic X-linked mental retardation. |
| Important Note | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| Background Descriptions | IQSEC2 is a 1,478 amino acid protein that belongs to the BRAG family and contains one IQ domain, one PH domain and a SEC7 domain. Localizing to the cytoplasm, IQSEC2 is expressed in brain, kidney and small intestine, with weaker levels of expression in placenta, pancreas, ovary, prostate and liver. IQSEC2 is a component of the postsynaptic density at excitatory synapses, and interacts with ARF family members as a guanine nucleotide exchange factor. Through the activation of ARF substrates, IQSEC2 may play a crucial role in cytoskeletal and synaptic organization. The gene encoding IQSEC2 maps to the human X chromosome. Defects to the IQSEC2 gene have been linked to mental retardation X-linked type 1 (MRX1), a condition characterized by decreased intellectual function. IQSEC2 exists as three isoforms due to alternative splicing events. |
| Gene ID | 23096 |
|---|---|
| Other Names | BRAG1; IQ-ArfGEF; MRX1; MRX18; MRX78; XLID1; IQEC2_HUMAN; IQSEC2; KIAA0522; IQ motif and Sec7 domain ArfGEF 2; mental retardation, X-linked 1 (non-dysmorphic); mental retardation, X-linked 78; mental retardation, X-linked 18; IQ motif and Sec7 domain 2; brefeldin A resistant Arf-guanine nucleotide exchange factor 1 |
| Dilution | IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500 |
| Storage | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
For Research Use Only. Not For Use In Diagnostic Procedures.
| Name | IQSEC2 (HGNC:29059) |
|---|---|
| Function | Is a guanine nucleotide exchange factor (GEF) for small GTPases of the ARF family, promoting activation of specific ARFs through exchange of GDP for GTP (PubMed:26793055, PubMed:37787765). In vitro, it has GEF activity towards ARF1 and ARF6 (PubMed:30842726, PubMed:37787765, PubMed:38200111). Is involved in the regulation of synaptic transmission and plasticity, controlling trafficking and removal of AMPA receptors GRIA2/GLUA2 and GRIA3/GLUA3 at synapses (PubMed:27009485, PubMed:30842726). Additionally, it may regulate the assembly of the post-synaptic density in a Ca(2+)-dependent manner, operating independently of its GEF activity (PubMed:41123449). |
| Cellular Location | Cell projection, dendritic spine {ECO:0000250|UniProtKB:Q5DU25}. Postsynaptic density |
| Tissue Location | Widely expressed. [Isoform 3]: Predominantly expressed in non-neural tissues. |
Research Areas
Application Protocols
Provided below are standard protocols that you may find useful for product applications.
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