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CD241 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT5284
产品名称
CD241 Rabbit Polyclonal Antibody
别名
RHAG; RH50; Ammonium transporter Rh type A; Erythrocyte membrane glycoprotein Rh50; Erythrocyte plasma membrane 50 kDa glycoprotein; Rh50A; Rhesus blood group family type A glycoprotein;Rh family type A glycoprotein; Rh type A glycoprotein; Rhesus blood group-associated ammonia channel; Rhesus blood group-associated glycoprotein; CD241
类别
常规抗体
基因名称
RHAG
蛋白名称
Ammonium transporter Rh type A
推荐应用
WB
反应种属
Human,Rat,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
6005
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6005
Human Swissprot No.
Q02094
Human Swissprot Link
http://www.uniprot.org/uniprotkb/Q02094/entry
Mouse Gene ID
19743
Mouse Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=19743
Mouse Swissprot No.
Q9QUT0
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q9QUT0
Rat Gene ID
65207
Rat Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=65207
Rat Swissprot No.
Q7TNK7
Rat Swissprot Link
http://www.uniprot.org/uniprot/Q7TNK7
免疫原
The antiserum was produced against synthesized peptide derived from the N-terminal region of human RHAG. AA range:1-50
特异性
CD241 Polyclonal Antibody detects endogenous levels of CD241 protein.
稀释度
WB 1:500 - 1:2000. IHC-p: 1:100-300 ELISA: 1:20000.. IF 1:50-200
预测分子量
44kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.[provided by RefSeq, Mar 2009],
组织表达
Erythrocytes.
细胞定位
Membrane ; Multi-pass membrane protein.
功能
disease:Defects in RHAG are the cause of regulator type Rh-null hemolytic anemia (RHN) [MIM:268150]; also called Rh-deficiency syndrome. RHN is a form of chronic hemolytic anemia in which the red blood cells have a stomatocytosis and spherocytosis morphology, an increased osmotic fragility, an altered ion transport system, and abnormal membrane phospholipid organization.,function:Associated with rhesus blood group antigen expression. May be part of an oligomeric complex which is likely to have a transport or channel function in the erythrocyte membrane.,similarity:Belongs to the ammonium transporter (TC 2.A.49) family. Rh subfamily.,subunit:Heterotetramer.,tissue specificity:Erythrocytes.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Western blot analysis of lysate from K562 cells, using RHAG Antibody.

Western Blot analysis of K562 cells using CD241 Polyclonal Antibody.. Secondary antibody was diluted at 1:20000

Immunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100

Immunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100

Immunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100

Immunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100

Immunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100

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