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人血红蛋白单克隆抗体
产品名称:
人血红蛋白单克隆抗体
英文名称:
hHb(H5A3)
产品类别:
抗体
产品编号:
Ysm-2118M
产品应用:
WB ELISA IHC-P
性状:
Liquid
纯化方法:
affinity purified by Protein A
保质期:
12个月
保存条件:
Shipped at 4℃. Store at -20 °C for one year. Avoid
[价格]
规格 价格 库存
50ul ¥ 1200 9
100ul ¥ 1900 5
200ul ¥ 2900 3

产品详情

 

产品编号 Ysm-2118M
英文名称 hHb(H5A3)
中文名称 人血红蛋白单克隆抗体
别    名 3-prime alpha-globin gene; Alpha globin; alpha one globin; alpha-1 globin; Alpha-globin; Beta globin; CD113t C; CD31; Erythremia, beta-globin type, included; Gamma 1 globin; Hb F Agamma; HBA 1; HBA 2; HBA; HBA_HUMAN; HBA1; HBA2; HBB; Hbb-y; HBD; Hbe1; HBG 1; HBG; HBG1; HBGA; HBGR; HBH; Hemoglobin alpha 1; hemoglobin alpha 1 globin chain; Hemoglobin alpha chain; Hemoglobin alpha locus; Hemoglobin alpha locus 1; hemoglobin alpha-1 chain; Hemoglobin beta; Hemoglobin beta chain; Hemoglobin beta chain complex; Hemoglobin beta locus; Hemoglobin gamma 1 chain; Hemoglobin gamma A; Hemoglobin gamma A chain; Hemoglobin gamma; Hemoglobin subunit alpha; Hemoglobin subunit beta; Hemoglobin subunit gamma 1; Hemoglobin--gamma locus, 136 alanaine; HSGGL1; LVV-hemorphin-7; Methemoglobinemia, beta-globin type, included; MGC126895; MGC126897; Minor alpha-globin locus; PRO2979

 

抗体来源 Mouse
克隆类型 Monoclonal
克 隆 号 H5A3
交叉反应 (predicted: Human, )
产品应用 WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 15.5kDa
细胞定位 细胞浆 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 human hemoglobin 
亚    型 IgG2a
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin; alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1; some nondeletion alpha thalassemias have also been reported. [provided by RefSeq, Jul 2008].

SWISS:
P68871

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