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血红蛋白β抗体
  • 产品货号：
    BN41337R
  • 中文名称：
    血红蛋白β抗体
  • 英文名称：
    Rabbit anti-Hemoglobin Beta Polyclonal antibody

  • 货号

    产品规格

    售价

    备注

  • BN41337R-100ul

    100ul

    ¥2360.00

    交叉反应：Human 推荐应用：WB,ELISA

  • BN41337R-200ul

    200ul

    ¥3490.00

    交叉反应：Human 推荐应用：WB,ELISA

英文名称Hemoglobin Beta
中文名称血红蛋白β抗体
别    名Beta 1 globin; beta globin; beta globin chain; BETA GLOBIN TYPE; BETA THALASSEMIAS; CD113t C; CD113t-C; ERYTHREMIA; HBB; Hemoglobin beta 1 chain; hemoglobin beta chain; hemoglobin beta chain complex; Hemoglobin beta chain, major form; HEMOGLOBIN BETA LOCUS; METHEMOGLOBINEMIA  
研究领域心血管  细胞生物  
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human, 
产品应用WB=1:500-2000 ELISA=1:5000-10000 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量15.5kDa
细胞定位细胞浆 分泌型蛋白 
性    状Liquid
浓    度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human Hemoglobin beta:51-147/147 
亚    型IgG
纯化方法affinity purified by Protein A
储 存 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.
PubMedPubMed
产品介绍The alpha (HBA) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult hemoglobin, Hb A. The normal adult hemoglobin tetramer consists of two alpha chains and two beta chains. Mutant beta globin causes sickle cell anemia. Absence of beta chain causes beta-zero-thalassemia. Reduced amounts of detectable beta globin causes beta-plus-thalassemia. The order of the genes in the beta-globin cluster is 5'-epsilon -- gamma-G -- gamma-A -- delta -- beta--3'. [provided by RefSeq, Jul 2008].

Function:
Involved in oxygen transport from the lung to the various peripheral tissues.

Tissue Specificity:
Red blood cells.

Post-translational modifications:
The initiator Met is not cleaved in variant Thionville and is acetylated.

DISEASE:
Defects in HBA1/HBA2 may be a cause of Heinz body anemias (HEIBAN) [MIM:140700]. This is a form of non-spherocytic hemolytic anemia of Dacie type 1. After splenectomy, which has little benefit, basophilic inclusions called Heinz bodies are demonstrable in the erythrocytes. Before splenectomy, diffuse or punctate basophilia may be evident. Most of these cases are probably instances of hemoglobinopathy. The hemoglobin demonstrates heat lability.
Heinz bodies are observed also with the Ivemark syndrome (asplenia with cardiovascular anomalies) and with glutathione peroxidase deficiency.


Similarity:
Belongs to the globin family.

SWISS:
P68871

Gene ID:
3043

Database links:

Entrez Gene: 3043 Human

Omim: 141900 Human

SwissProt: P68871 Human

Unigene: 523443 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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