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AB156584

Anti-fetal hemoglobin antibody [EPR9709]

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(2 Publications)

Rabbit Recombinant Monoclonal HBG1 antibody. Suitable for WB and reacts with Human samples. Cited in 2 publications.

View Alternative Names

PRO2979, HBG1, Hemoglobin subunit gamma-1, Gamma-1-globin, Hb F Agamma, Hemoglobin gamma-1 chain, Hemoglobin gamma-A chain

1 Images
Western blot - Anti-fetal hemoglobin antibody [EPR9709] (AB156584)
  • WB

Unknown

Western blot - Anti-fetal hemoglobin antibody [EPR9709] (AB156584)

Blocking and Diluting buffer : 5% NFDM/TBST

Exposure time : 3 min

All lanes:

Western blot - Anti-fetal hemoglobin antibody [EPR9709] (ab156584) at 1/2000 dilution

Lane 1:

Human red blood cell at 20 µg

Lane 2:

K562(human lymphoblast from chronic myelogenous leukemia) whole cell lysate at 20 µg

Secondary

All lanes:

Goat Anti-Rabbit IgG H&L (HRP) at 1/1000 dilution

Predicted band size: 16 kDa

false

  • Carrier free

    Anti-fetal hemoglobin antibody [EPR9709] - BSA and Azide free

Key facts

Host species

Rabbit

Clonality

Monoclonal

Clone number

EPR9709

Isotype

IgG

Carrier free

No

Reacts with

Human

Applications

WB

applications

Immunogen

The exact immunogen used to generate this antibody is proprietary information.

Specificity

ab156584 recognises Hemoglobin gamma-1/2 chain.

Reactivity data

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Product details

Species reactivity
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species.
Please contact us for more information.

Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:

  • - High batch-to-batch consistency and reproducibility
  • - Improved sensitivity and specificity
  • - Long-term security of supply
  • - Animal-free batch production

For more information, read more on recombinant antibodies.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein A
Storage buffer
pH: 7.2 - 7.4 Preservative: 0.01% Sodium azide Constituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Shipped at conditions
Conditional Ambient
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Fetal hemoglobin also known as fetal Hb or HbF is a form of hemoglobin found in fetuses and neonates. HbF is composed of two alpha and two gamma globin chains and its molecular weight is around 64000 Daltons. This hemoglobin variant is mainly expressed in the red blood cells of the fetal liver and bone marrow. Expression of fetal hemoglobin typically declines after birth when beta globin chains replace gamma chains to form adult hemoglobin (HbA). However low levels of fetal hemoglobin can persist into adulthood in some individuals.
Biological function summary

Fetal hemoglobin has a higher affinity for oxygen compared to adult hemoglobin. This characteristic allows efficient transfer of oxygen from maternal to fetal circulation which is vital for fetal development. Fetal hemoglobin is not part of any complex but its unique structure is adapted to its function in the fetal environment. The alpha and gamma globin chains together modulate its oxygen-binding properties ensuring proper oxygenation during fetal life.

Pathways

The production and transition of fetal hemoglobin are linked to the globin gene switching pathway. This process involves the silencing of gamma globin genes and activation of beta globin genes postnatally a transition integral to producing adult hemoglobin. BCL11A and KLF1 are transcription factors that play essential roles in regulating this gene switching. Both proteins influence the repression of gamma globin genes therefore promoting the expression of beta globin.

Fetal hemoglobin is significant in conditions like sickle cell disease and beta thalassemia. In these disorders elevated levels of fetal hemoglobin can ameliorate symptoms by compensating for defective adult hemoglobin. Patients with higher fetal hemoglobin levels typically exhibit milder forms of these diseases. Therapeutic approaches aim to reactivate fetal hemoglobin expression through the modulation of proteins like BCL11A KLF1 and others involved in hemoglobin switching.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Gamma chains make up the fetal hemoglobin F, in combination with alpha chains.
See full target information HBG1

Publications (2)

Recent publications for all applications. Explore the full list and refine your search

Molecular medicine reports 31: PubMed39450557

2024

Upregulation of miR‑6747‑3p affects red blood cell lineage development and induces fetal hemoglobin expression by targeting BCL11A in β‑thalassemia.

Applications

Unspecified application

Species

Unspecified reactive species

Aixiang Lv,Meihuan Chen,Siwen Zhang,Wantong Zhao,Jingmin Li,Siyang Lin,Yanping Zheng,Na Lin,Liangpu Xu,Hailong Huang

Clinical and translational medicine 5:15 PubMed27056246

2016

Hydroxyurea down-regulates BCL11A, KLF-1 and MYB through miRNA-mediated actions to induce γ-globin expression: implications for new therapeutic approaches of sickle cell disease.

Applications

WB

Species

Human

Gift Dineo Pule,Shaheen Mowla,Nicolas Novitzky,Ambroise Wonkam
View all publications

Product promise

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