CERKL 抗体 (AA 65-160)
-
- 抗原 See all CERKL 抗体
- CERKL (Ceramide Kinase-Like (CERKL))
-
抗原表位
- AA 65-160
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This CERKL antibody is un-conjugated
-
应用范围
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat,Sheep
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CAMK1D
- 亚型
- IgG
- Top Product
- Discover our top product CERKL Primary Antibody
-
-
- 应用备注
-
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
-
- 抗原
- CERKL (Ceramide Kinase-Like (CERKL))
- 别名
- CERKL (CERKL 产品)
- 别名
- RGD1561057 antibody, Gm1958 antibody, Rp26 antibody, GB19002 antibody, RP26 antibody, zgc:162213 antibody, ceramide kinase like antibody, ceramide kinase-like antibody, ceramide kinase antibody, CERKL antibody, Cerkl antibody, LOC408315 antibody, CERK antibody, LOC100566923 antibody, LOC100645684 antibody, cerkl antibody
- 背景
-
Synonyms: Ceramide kinase like protein, Ceramide kinase-like protein, CERKL, CERKL_HUMAN, Retinitis pigmentosa 26 autosomal recessive, RP26.
Background: This gene was initially identified as a locus (RP26) associated with an autosomal recessive form of retinitis pigmentosa (arRP) disease. This gene encodes a protein with ceramide kinase-like domains, however, the protein does not phosphorylate ceramide and its target substrate is currently unknown. This protein may be a negative regulator of apoptosis in photoreceptor cells. Mutations in this gene cause a form of retinitis pigmentosa characterized by autosomal recessive cone and rod dystrophy (arCRD). Alternative splicing of this gene results in multiple transcript variants encoding different isoforms and non-coding transcripts.[provided by RefSeq, May 2010].
-