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SLC25A46 Polyclonal antibody

SLC25A46 Polyclonal Antibody for WB, ELISA
Cat No. 12277-1-AP

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human, mouse, rat

应用

WB, ELISA and More (1)

SLC25A46, TB1

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  Unconjugated
Unconjugated
规格: 

-/ -


经过测试的应用

Positive WB detected inJurkat cells, mouse brain tissue, rat brain tissue

推荐稀释比

应用推荐稀释比
Western Blot (WB)WB : 1:500-1:3000
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

12277-1-AP targets SLC25A46 in WB, IF, ELISA applications and shows reactivity with human, mouse, rat samples.

经测试应用 WB, ELISA Application Description
文献引用应用WB, IF
经测试反应性 human, mouse, rat
文献引用反应性human, rat
免疫原 SLC25A46 fusion protein Ag2923 种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Polyclonal
产品类型 Antibody
全称 solute carrier family 25, member 46
别名 SLC25A46, TB1
计算分子量 418 aa, 46 kDa
观测分子量 46 kDa
GenBank蛋白编号BC017169
基因名称 SLC25A46
Gene ID (NCBI) 91137
RRIDAB_2239384
偶联类型 Unconjugated
形式 Liquid
纯化方式Antigen affinity purification
UNIPROT IDQ96AG3
储存缓冲液 PBS with 0.02% sodium azide and 50% glycerol , pH 7.3
储存条件Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

SLC25A46 belongs to the SLC25 family of mitochondrial carrier proteins.

实验方案

Product Specific Protocols
WB protocol for SLC25A46 antibody 12277-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

发表文章

SpeciesApplicationTitle
humanWB

Cell Metab

A High-Density Human Mitochondrial Proximity Interaction Network.

Authors - Hana Antonicka
WB

Sci Adv

Global ubiquitylation analysis of mitochondria in primary neurons identifies endogenous Parkin targets following activation of PINK1.

Authors - Odetta Antico
humanWB,IF

Brain

Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia.

Authors - Jijun Wan
humanWB

EMBO Mol Med

SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome.

Authors - Alexandre Janer
  • KD Validated
humanWB

J Pers Med

Reanalysis of Exome Data Identifies Novel SLC25A46 Variants Associated with Leigh Syndrome.

Authors - Qifei Li
humanWB

Mol Biol Cell

Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2 mediated hyperfusion of mitochondria.

Authors - Janos Steffen
  • KO Validated
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