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Mouse Anti-hHb(H5A3)/Gold Conjugated antibody (bsm-2118M-Gold)
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說(shuō) 明 書(shū): 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bsm-2118M-Gold
英文名稱 Mouse Anti-hHb(H5A3)/Gold Conjugated antibody
中文名稱 膠體金標(biāo)記的小鼠抗人血紅蛋白單克隆抗體
別    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 l  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買(mǎi)        大包裝/詢價(jià)
說(shuō) 明 書(shū) 100ul(10nm  15nm  35nm
研究領(lǐng)域 免疫學(xué)  
抗體來(lái)源 Mouse
克隆類型 Monoclonal
克 隆 號(hào) H5A3
交叉反應(yīng) (predicted: Human, )
產(chǎn)品應(yīng)用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 15.5kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 human hemoglobin
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產(chǎn)品介紹 background:
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].

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



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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