C19orf12 Polyclonal antibody

C19orf12 Polyclonal Antibody for WB, IHC, ELISA
Cat No. 27382-1-AP

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human

应用

WB, IHC, ELISA

Protein C19orf12

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  Unconjugated
Unconjugated
规格价格库存


经过测试的应用

Positive WB detected inU2OS cells
Positive IHC detected inhuman stomach cancer 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

应用推荐稀释比
Western Blot (WB)WB : 1:150-1:600
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

27382-1-AP targets C19orf12 in WB, IHC, ELISA applications and shows reactivity with human samples.

经测试应用 WB, IHC, ELISA Application Description
文献引用应用WB
经测试反应性 human
文献引用反应性human
免疫原 C19orf12 fusion protein Ag26555 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 chromosome 19 open reading frame 12
别名 Protein C19orf12
计算分子量 107 aa, 11 kDa
观测分子量 20 kDa
GenBank蛋白编号BC063518
基因名称 C19orf12
Gene ID (NCBI) 83636
RRIDAB_2880858
偶联类型 Unconjugated
形式 Liquid
纯化方式Antigen affinity purification
UNIPROT IDQ9NSK7
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.

实验方案

Product Specific Protocols
WB protocol for C19orf12 antibody 27382-1-APDownload protocol
IHC protocol for C19orf12 antibody 27382-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

发表文章

SpeciesApplicationTitle
humanWB

Free Radic Biol Med

C19orf12 ablation causes ferroptosis in mitochondrial membrane protein-associated with neurodegeneration.

Authors - Changjuan Shao
humanWB

Nat Metab

A spatiotemporal proteomic map of human adipogenesis

Authors - Felix Klingelhuber
  • KD Validated
humanWB

Stem Cell Res

Generation of four human induced pluripotent stem cell lines derived from patients with MPAN, subtype of NBIA, carrying the c.204_214del11 mutation in the C19orf12 gene

Authors - Ewelina Krogulec
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