HBG1 rabbit pAb

HBG1 rabbit pAb

AO-06-ES15816-100

HBG1 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES15816
Product nameHBG1 rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB
Other name
Size100μL
Unit price ($)248
Human gene ID3047
Human Swiss-ProtP69891
SourceRabbit
IsotypeIgG
TargetHBG1
Fields
Gene nameHBG1 PRO2979
Protein nameHBG1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-Prot
Mouse Swiss link
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenSynthesized peptide derived from human HBG1 AA range: 34-84
SpecificityThis antibody detects endogenous levels of HBG1 at Human
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)16kD
Observed band (KD)
BackgroundThe gamma globin genes (HBG1 and HBG2) are normally expressed in the fetal liver, spleen and bone marrow. Two gamma chains together with two alpha chains constitute fetal hemoglobin (HbF) which is normally replaced by adult hemoglobin (HbA) at birth. In some beta-thalassemias and related conditions, gamma chain production continues into adulthood. The two types of gamma chains differ at residue 136 where glycine is found in the G-gamma product (HBG2) and alanine is found in the A-gamma product (HBG1). The former is predominant at birth. 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],
Functiondevelopmental stage:Expressed until four or five weeks after birth.,disease:Some gamma variants can cause severe jaundice and cyanosis in premature and new born babies.,function:Gamma chains make up the fetal hemoglobin F, in combination with alpha chains.,online information:Human hemoglobin variants and thalassemias,PTM:Acetylation of Gly-2 converts Hb F to the minor Hb F1.,similarity:Belongs to the globin family.,subunit:Heterotetramer of two alpha chains and two gamma chains in fetal hemoglobin (Hb F). In the case of deletions affecting one or more of the alpha chains the excess gamma chains form homotetramers that exhibit neither Bohr effect nor heme-heme cooperativity (hemoglobin Bart's).,tissue specificity:Red blood cells.,
Subcellular locationcytosol,hemoglobin complex,
ExpressionRed blood cells.

Additional Images

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Western blot analysis of lysates from A431 cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES15816-100
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Hurry! only 10 items left in stock.

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