NSRRC TPS13A standard protein archive

Orion Shih.

SASDRN8 – α/β Hemoglobin (human)

Hemoglobin subunit alpha
Hemoglobin subunit beta
MWexperimental 63 kDa
MWexpected 63 kDa
VPorod 97 nm3
log I(s) 5.87×10-1 5.87×10-2 5.87×10-3 5.87×10-4
Hemoglobin subunit alpha Hemoglobin subunit beta small angle scattering data  s, nm-1
ln I(s)
Hemoglobin subunit alpha Hemoglobin subunit beta Guinier plot ln 5.88×10-1 Rg: 2.5 nm 0 (2.5 nm)-2 s2
(sRg)2I(s)/I(0)
Hemoglobin subunit alpha Hemoglobin subunit beta Kratky plot 1.104 0 3 sRg
p(r)
Hemoglobin subunit alpha Hemoglobin subunit beta pair distance distribution function Rg: 2.5 nm 0 Dmax: 9.2 nm

Data validation


There are no models related to this curve.

Synchrotron SAXS data from solutions of α/β hemoglobin in phosphate buffered saline, pH 7.5 were collected on the 13A beam line at the Taiwan Photon Source (NSRRC, Hsinchu, Taiwan) using a Eiger X 1M and Eiger X 9M detector at a sample-detector distance of 1.3 m and at a wavelength of λ = 0.083 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 100.00 μl sample at 20 mg/ml was injected at a 0.20 ml/min flow rate onto a GE Superdex 200 Increase 5/150 column at 10°C. Five successive 2 second frames were collected. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.

Hemoglobin subunit alpha (Hba)
Mol. type   Protein
Organism   Homo sapiens
Olig. state   Dimer
Mon. MW   15.3 kDa
 
UniProt   P69905 (1-142)
Sequence   FASTA
 
Hemoglobin subunit beta (Hbb)
Mol. type   Protein
Organism   Homo sapiens
Olig. state   Dimer
Mon. MW   16.0 kDa
 
UniProt   P68871 (1-147)
Sequence   FASTA