DATASHEET
Host:
Rabbit
Target Protein:
HBA1
Clonality:
Recombinant
Isotype:
IgG
Entrez Gene:
3039
Swiss Prot:
P69905
Source:
KLH conjugated synthetic peptide derived from human HBA1
Purification:
Purified by Protein A.
Storage Buffer:
Aqueous buffered solution containing 0.01M TBS (pH 7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Storage:
Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
Background:
he 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]
Conjugation:
Cy5
Excitation/ Emission:
625,650nm/670nm
Size:
100µL
Concentration:
Lot Dependent
Applications:
IF(IHC-P)(IF(IHC-P)(1:50-200))
15
Mouse
Rat
For research use only. Not intended for diagnostic or therapeutic use.