验证数据展示
经过测试的应用
Positive WB detected in | HEK-293 cells, HepG2 cells, HeLa cells, mouse brain tissue, rat brain tissue |
Positive IHC detected in | mouse heart tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
推荐稀释比
Application | Dilution |
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Western Blot (WB) | WB : 1:500-1:2000 |
Immunohistochemistry (IHC) | IHC : 1:50-1:500 |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
产品信息
28341-1-AP targets MFN2 in WB, IHC, ELISA applications and shows reactivity with Human, Mouse, Rat samples.
Tested Applications | WB, IHC, ELISA Application Description |
Tested Reactivity | Human, Mouse, Rat |
Immunogen | MFN2 fusion protein Ag28128 种属同源性预测 |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Type | Antibody |
Full Name | mitofusin 2 |
Synonyms | CMT2A, CMT2A2, CPRP1, HSG, KIAA0214, MARF, MFN2, mitofusin 2, Transmembrane GTPase MFN2 |
Calculated Molecular Weight | 757 aa, 86 kDa |
Observed Molecular Weight | 86 kDa |
GenBank Accession Number | BC017061 |
Gene Symbol | MFN2 |
Gene ID (NCBI) | 9927 |
ENSEMBL Gene ID | ENSG00000116688 |
RRID | AB_2881116 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Antigen affinity purification |
UNIPROT ID | O95140 |
Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
MFN2, also named as CPRP1 and KIAA0214, belongs to the mitofusin family. It is an Essential transmembrane GTPase, which mediates mitochondrial fusion. MFN2 acts independently of the cytoskeleton. It therefore plays a central role in mitochondrial metabolism and may be associated with obesity and/or apoptosis processes. Overexpression of MFN2 induces the formation of mitochondrial networks. It plays an important role in the regulation of vascular smooth muscle cell proliferation. Defects in MFN2 are the cause of Charcot-Marie-Tooth disease type 2A2 (CMT2A2). Defects in MFN2 are the cause of Charcot-Marie-Tooth disease type 6 (CMT6). Ubiquitinated forms of Mfn2 (mono- and polyubiquitinated) are present during mitophagy.
实验方案
Product Specific Protocols | |
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WB protocol for MFN2 antibody 28341-1-AP | Download protocol |
IHC protocol for MFN2 antibody 28341-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |