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Catalog: YM0523
Size
Price
Status
Qty.
200μL
$600.00
3 weeks

0

100μL
$350.00
3 weeks

0

50μL
$210.00
3 weeks

0

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Main Information
Target

PLZF

Host Species

Mouse

Reactivity

Human

Applications

WB, IF, ELISA

MW

74kD (Calculated)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:500-1:2000; IF 1:200-1:1000; ELISA 1:10000; Not yet tested in other applications.
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
PLZF Monoclonal Antibody detects endogenous levels of PLZF protein.
Purification
Affinity purification
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
MW(Calculated)
74kD
Modification
Unmodified
Clonality
Monoclonal
Clone Number
11A9
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Antigen&Target Information
Immunogen:
Purified recombinant fragment of human PLZF expressed in E. Coli.
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Specificity:
PLZF Monoclonal Antibody detects endogenous levels of PLZF protein.
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Gene Name:
ZBTB16
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Protein Name:
Zinc finger and BTB domain-containing protein 16
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Other Name:
ZBTB16 ;
PLZF ;
ZNF145 ;
Zinc finger and BTB domain-containing protein 16 ;
Promyelocytic leukemia zinc finger protein ;
Zinc finger protein 145 ;
Zinc finger protein PLZF
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Database Link:
Organism Gene ID SwissProt
Human 7704; Q05516;
Background:
This gene is a member of the Krueppel C2H2-type zinc-finger protein family and encodes a zinc finger transcription factor that contains nine Kruppel-type zinc finger domains at the carboxyl terminus. This protein is located in the nucleus, is involved in cell cycle progression, and interacts with a histone deacetylase. Specific instances of aberrant gene rearrangement at this locus have been associated with acute promyelocytic leukemia (APL). Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008],
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Function:
Disease:A chromosomal aberration involving ZBTB16 may be a cause of acute promyelocytic leukemia (APL). Translocation t(11;17)(q32;q21) with RARA.,Disease:Defects in ZBTB16 are the cause of skeletal defects genital hypoplasia and mental retardation [MIM:612447]. The disorder is characterized by mental retardation, craniofacial dysmorphism, microcephaly and short stature. Additional features include absence of the thumbs, hypoplasia of the radii and ulnae, additional vertebrae and ribs, retarded bone age and genital hypoplasia.,Function:Probable transcription factor. May play a role in myeloid maturation and in the development and/or maintenance of other differentiated tissues. Probable substrate-recognition component of an E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins.,induction:By retinoic acid.,pathway:Protein modification; protein ubiquitination.,similarity:Belongs to the krueppel C2H2-type zinc-finger protein family.,similarity:Contains 1 BTB (POZ) domain.,similarity:Contains 9 C2H2-type zinc fingers.,subunit:Binds EPN1. Interacts with ZBTB32 and CUL3.,tissue specificity:Within the hematopoietic system, PLZF is expressed in bone marrow, early myeloid cell lines and peripheral blood mononuclear cells. Also expressed in the ovary, and at lower levels, in the kidney and lung.,
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Cellular Localization:
Nucleus . Nucleus, nuclear body .
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Research Areas:
>>Pathways in cancer ;
>>Transcriptional misregulation in cancer ;
>>Acute myeloid leukemia
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Catalog: YM0523
Size
Price
Status
Qty.
200μL
$600.00
3 weeks

0

100μL
$350.00
3 weeks

0

50μL
$210.00
3 weeks

0

Add to cart

Collected

Collect

Customized Service

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