AFF1 Polyclonal Antibody
€0.00
In stock
SKU
E-AB-61412
Catalog Number: E-AB-61412
Isotype: Rabbit IgG
Reactivity: human,rat
Applications: IF
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human,rat
Applications: IF
Datasheet, Questions? Contact us!
Background:
This gene encodes a member of the AF4/ lymphoid nuclear protein related to AF4/Fragile X E mental retardation syndrome family of proteins, which have been implicated in childhood lymphoblastic leukemia, Fragile X E site mental retardation, and ataxia. It is the prevalent mixed-lineage leukemia fusion gene associated with spontaneous acute lymphoblastic leukemia. Members of this family have three conserved domains: an N-terminal homology domain, an AF4/ lymphoid nuclear protein related to AF4/Fragile X E mental retardation syndrome domain, and a C-terminal homology domain. The protein functions as a regulator of RNA polymerase II-mediated transcription through elongation and chromatin remodeling functions. Through RNA interference screens, this gene has been shown to promote the expression of CD133, a plasma membrane glycoprotein required for leukemia cell survival. Alternative splicing results in multiple transcript variants.
Research Area: Cancer, Epigenetics and Nuclear Signaling
Synonyms:
AFF1, AF4, MLLT2, PBM1
Immunogen: Recombinant fusion protein of human AFF1 (NP_001160165.1).
Swissprot: P51825
Gene ID: 4299
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: IF 1:50-1:100
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
This gene encodes a member of the AF4/ lymphoid nuclear protein related to AF4/Fragile X E mental retardation syndrome family of proteins, which have been implicated in childhood lymphoblastic leukemia, Fragile X E site mental retardation, and ataxia. It is the prevalent mixed-lineage leukemia fusion gene associated with spontaneous acute lymphoblastic leukemia. Members of this family have three conserved domains: an N-terminal homology domain, an AF4/ lymphoid nuclear protein related to AF4/Fragile X E mental retardation syndrome domain, and a C-terminal homology domain. The protein functions as a regulator of RNA polymerase II-mediated transcription through elongation and chromatin remodeling functions. Through RNA interference screens, this gene has been shown to promote the expression of CD133, a plasma membrane glycoprotein required for leukemia cell survival. Alternative splicing results in multiple transcript variants.
Research Area: Cancer, Epigenetics and Nuclear Signaling
Synonyms:
AFF1, AF4, MLLT2, PBM1
Immunogen: Recombinant fusion protein of human AFF1 (NP_001160165.1).
Swissprot: P51825
Gene ID: 4299
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: IF 1:50-1:100
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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