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RHCE Rabbit pAb (bs-5956R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-5956R
英文名稱 RHCE Rabbit pAb
中文名稱 Rh血型C抗原抗體
別    名 Blood group Rh(CE) polypeptide; Blood group RhCcEe antigen; CD240CE; CD240CE antigen; RH; Rh blood group antigen Evans; Rh blood group C antigen; Rh blood group, CcEe antigens; Rh polypeptide 1; Rh polypeptide I; RH30A; Rh4; RHC; RHCE blood group variant Crawford antigen Rh43; RHE; Rhesus blood group CE protein; Rhesus blood group E antigen; Rhesus blood group Rhce antigen; Rhesus blood group, CcEe antigens; Rhesus C/E antigens; Rhesus system C and E polypeptides; RhIVb(J); RHIXB; RHPI; RhVI; RhVIII; RHCE_HUMAN.  
研究領(lǐng)域 腫瘤  心血管  免疫學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  G蛋白信號(hào)  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human)
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 46 kDa
檢測(cè)分子量
細(xì)胞定位 細(xì)胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human RHCE: 2-120/417 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項(xiàng) This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 The Rh blood group system is the second most clinically significant of the blood groups, second only to ABO. It is also the most polymorphic of the blood groups, with variations due to deletions, gene conversions, and missense mutations. The Rh blood group includes this gene which encodes both the RhC and RhE antigens on a single polypeptide and a second gene which encodes the RhD protein. The classification of Rh-positive and Rh-negative individuals is determined by the presence or absence of the highly immunogenic RhD protein on the surface of erythrocytes. A mutation in this gene results in amorph-type Rh-null disease. There are thirteen named isoforms.

Function:
May be part of an oligomeric complex which is likely to have a transport or channel function in the erythrocyte membrane.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
Restricted to tissues or cell lines expressing erythroid characters. Isoform 4g and isoform RhPI-Alpha are expressed in immature erythroblasts but not in mature erythroblasts.

Similarity:
Belongs to the ammonium transporter (TC 2.A.49) family. Rh subfamily.

SWISS:
P18577

Gene ID:
6006

Database links:

Entrez Gene: 6006 Human

Omim: 111700 Human

SwissProt: P18577 Human



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