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hHb Mouse mAb (bsm-2118M)  
訂購(gòu)熱線(xiàn):400-901-9800
訂購(gòu)郵箱:sales@bioss.com.cn
訂購(gòu)QQ:  400-901-9800
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
200ug(PBS only)/5600.00元
大包裝/詢(xún)價(jià)
產(chǎn)品編號(hào) bsm-2118M
英文名稱(chēng) hHb Mouse mAb
中文名稱(chēng) 人血紅蛋白單克隆抗體
別    名 Hemoglobin subunit alpha; HBA1; HBA2; Alpha-globin;Hemoglobin alpha chain;Hemoglobin subunit beta; Beta-globin; Hemoglobin beta chain; Hemoglobin subunit gamma-1; Gamma-1-globin; Hb F Agamma; Hemoglobin gamma-1 chain; Hemoglobin gamma-A chain; HBG1; HBD;   
Specific References  (1)     |     bsm-2118M has been referenced in 1 publications.
[IF=3.7] Liu, Cui-Mei, et al. "Specific detection of latent human blood fingerprints using antibody modified NaYF 4: Yb, Er, Gd fluorescent upconversion nanorods." Dyes and Pigments (2017).  other ;  Human.  
研究領(lǐng)域 心血管  細(xì)胞類(lèi)型標(biāo)志物  
抗體來(lái)源 Mouse
克隆類(lèi)型 Monoclonal
克 隆 號(hào) H5A3
交叉反應(yīng) (predicted: Human)
產(chǎn)品應(yīng)用 WB=1:500-2000,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 15.5 kDa
檢測(cè)分子量
細(xì)胞定位 細(xì)胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 human hemoglobin 
亞    型 IgG2a
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 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:
P69905

Gene ID:
3039

Database links:

Entrez Gene: 3039 Human

Entrez Gene: 3040 Human

Entrez Gene: 3047 Human

Omim: 141800 Human

Omim: 141900 Human

Omim: 142200 Human

SwissProt: P68871 Human

SwissProt: P69891 Human

SwissProt: P69905 Human

Unigene: 449630 Human

Unigene: 523443 Human

Unigene: 654744 Human



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