Home > Product > Antibody > Rabbit Anti-Thrombopoietin/FITC Conjugated antibody
c mpl ligand; C-mpl ligand; Megakaryocyte Colony Stimulating Factor; Megakaryocyte colony-stimulating factor; Megakaryocyte growth and development factor; Megakaryocyte stimulating factor; MGDF; MKCSF; ML; MPL ligand; MPLLG; Myeloproliferative Leukemia Vi
Cat:
SL10407R-FITC
Species Reactivity:
Human,Mouse,Rat,(predicted: Cow,Sheep,)
Immunogen:
KLH conjugated synthetic peptide derived from human Thrombopoietin
Format:
Lyophilized or Liquid
Storage instructions:
Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of ant
Buffer:
0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Concentration:
1mg/ml
Clonality:
Polyclonal
Isotype:
IgG
Applications:
ICC=1:50-200IF=1:50-200not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.
Host:
Rabbit
Calculated MW:
37kDa
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Unit:
Price: $
Product PDFs
Datasheet:


background:
Megakaryocytopoiesis is the cellular development process that leads to platelet production. The protein encoded by this gene is a humoral growth factor that is necessary for megakaryocyte proliferation and maturation, as well as for thrombopoiesis. This protein is the ligand for MLP/C_MPL, the product of myeloproliferative leukemia virus oncogene. Mutations in this gene are the cause of thrombocythemia 1. Alternate splicing results in multiple transcript variants of this gene.[provided by RefSeq, Jun 2012].

Function:
Lineage-specific cytokine affecting the proliferation and maturation of megakaryocytes from their committed progenitor cells. It acts at a late stage of megakaryocyte development. It may be the major physiological regulator of circulating platelets.

Subcellular Location:
Secreted.

DISEASE:
Thrombocythemia 1 (THCYT1) [MIM:187950]: A myeloproliferative disorder characterized by excessive platelet production, resulting in increased numbers of circulating platelets. It can be associated with spontaneous hemorrhages and thrombotic episodes. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the EPO/TPO family.

Database links:

Entrez Gene: 7066 Human

Entrez Gene: 21832 Mouse

Entrez Gene: 81811 Rat

Omim: 600044 Human

SwissProt: P40225 Human

SwissProt: P40226 Mouse

SwissProt: P49745 Rat

Unigene: 1166 Human

Unigene: 3943 Mouse

Unigene: 10576 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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