Below is the resulting gel for this experiment. QUO strloton lo toz qutoi deno 1 2 3 4

biliverdin                macrophages                 urobilinogen                       bilirubin Erythrocytes are continually replaced. Worn-out erythrocytes are lysed in the spleen as they pass through splenic cords in the spleen.   Blank 1  digest these cell parts, and separate heme from the globin units of hemoglobin. The globin proteins are broken down into amino acids and recycled. The heme pigment is converted into Blank 2 , then Blank 3 , and released into the blood. It is concentrated in urine, producing its yellow color. The liver removes additional bilirubin and secretes it into bile. When released into the small intestine, bacteria transform it into Blank 4 , which makes feces brown.

The part of hemoglobin that binds iron is O alpha globulin 2 Obeta globulin 2 alpha globulin 1 O beta globulin 1 heme

Answer the following questions about hemoglobin. The number of high affinity binding sites in the R form of hemoglobin is       .The number of low affinity binding sites in the R form of hemoglobin is       .The number of O2 molecules that need to bind to convert hemoglobin from the T to R form is       .The number of high affinity binding sites in the T form of hemoglobin is       .The number of low affinity binding sites in the T form of hemoglobin is

3

The vaccine for Haemophilus influenzae type b is called a conjugate vaccine. It is composed of the tetanus toxoid protein conjugated to the capsular polysaccharide of the H. influenzae type b bacteria. When used to vaccinate infants, the antibody response generated by this vaccine would include 0 0 0 0 antibodies that bind only to the protein-polysaccharide conjugate in the vaccine. antibodies to the tetanus toxoid only. antibodies to the bacterial polysaccharide and the tetanus toxoid. antibodies to the bacterial polysaccharide only.

I know that hemoglobin has cooperative  binding what about hemocyanin does it have cooperative binding

please choose only one option i can only choose one

The doctor also mentioned a new treatment for Sickle Cell Disease to JJ called Voxelotor (Oxbryta). Voxelotor binds to the a-globin chain and alters the structure of HbS stabilizing it in the R-state (relaxed state). Q7: In the presence of Voxelotor would you expect the affinity of HbS for O2 to increase or decrease? Q8: How would you classify the mechanism of action for Voxelotor?

Identify the human form of hemoglobin that is produced only by the embryo. two a-globin chains (alpha) and two b-globin chains (beta) two b-globin chains (beta) and two g-globin chains (gamma) two g-globin chains (gamma) and two d-globin chains (delta) two d-globin chains (delta) and two e-globin chains (epsilon) two e-globin chains (epsilon) and two z-globin chains (zeta)