Western Blot: PRDM16/MEL1 Antibody [NBP1-77096] - Analysis of PRDM16 in K562 cell lysate with PRDM16 antibody at 1 ug/mL.
Immunocytochemistry/ Immunofluorescence: PRDM16/MEL1 Antibody - BSA Free [NBP1-77096] - Immunofluorescence of PRDM16/MEL1 in Human Brain cells with PRDM16/MEL1 antibody at 20 u/mL.
Immunohistochemistry: PRDM16/MEL1 Antibody - BSA Free [NBP1-77096] - Immunohistochemistry of PRDM16/MEL1 in human brain tissue with PRDM16/MEL1 antibody at 2 u/ml.
Immunocytochemistry/ Immunofluorescence: PRDM16/MEL1 Antibody - BSA Free [NBP1-77096] - Immunofluorescence of PRDM16/MEL1 in mouse brain tissue with PRDM16/MEL1 antibody at 20 u/ml.Green: PRDM16/MEL1 Antibody Blue: ...read more
Immunohistochemistry: PRDM16/MEL1 Antibody - BSA Free [NBP1-77096] - Immunohistochemistry of PRDM16/MEL1 in mouse brain tissue with PRDM16/MEL1 antibody at 2 u/ml.
Antibody was raised against a 17 amino acid synthetic peptide from near the carboxy terminus of human PRDM16. The immunogen is located within amino acids 1120 - 1170 of PRDM16. Amino Acid Squence: AGKSQDDTVSPAPEPQA
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
PRDM16
Purity
Peptide affinity purified
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140 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
PBS
Preservative
0.02% Sodium Azide
Concentration
1 mg/ml
Purity
Peptide affinity purified
Alternate Names for PRDM16/MEL1 Antibody - BSA Free
MDS1/EVI1-like gene 1
MEL1
MEL1KIAA1675PFM13MGC166915
PFM13
PR domain containing 16
PR domain zinc finger protein 16
PR domain-containing protein 16
PRDM16
Transcription factor MEL1
Background
PRDM16 is a zinc finger transcription factor and contains an N-terminal PR domain. The reciprocal translocation t(1;3)(p36;q21) occurs in a subset of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). This gene is located near the 1p36.3 breakpoint and has been shown to be specifically expressed in the t(1:3)(p36,q21)-positive MDS/AML. The translocation results in the overexpression of a truncated version of this protein that lacks the PR domain, which may play an important role in the pathogenesis of MDS and AML. Recent studies have shown that PRDM16 normally acts as a Smad3 binding protein that may be important for the development of orofacial structures through modulation of the TGF-beta signaling pathway. Other experiments have indicated that PRDM16 controls a bidirectional cell fate switch between skeletal myoblasts and brown fat cells.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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