Search :
Sign in or Register  
Welcome Sign in or Don't have an account?Register

Mouse Anti-BCL11A Recombinant Antibody (H1) (CBMAB-1199-CN)

Online Inquiry
Published Data

Summary

Host Animal
Mouse
Specificity
Human, Mouse, Rat
Clone
H1
Antibody Isotype
IgG2a, κ
Application
WB, IP, IF, ELISA

Basic Information

Immunogen
Amino acids 505-620 mapping within an internal region of Bcl-11a of human origin.
Host Species
Mouse
Specificity
Human, Mouse, Rat
Antibody Isotype
IgG2a, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.
ApplicationNote
WB1:100-1:1,000
IP1-2 µg per 100-500 µg of total protein (1 ml of cell lysate)
IF(ICC)1:50-1:500
ELISA1:100-1:1,000

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS, 0.1% gelatin
Preservative
< 0.1% sodium azide
Concentration
0.2 mg/ml
Storage
Store at +4°C.
Epitope
Localized in aa. 172-434

Target

Full Name
B Cell CLL/Lymphoma 11A
Introduction
B-cell lymphoma/leukemia 11A (BCL11A) is a C2H2 type zinc-finger protein by its similarity to the mouse Bcl11a/Evi9 protein. BCL11A has been found to play a role in the suppression of fetal hemoglobin production. Therapeutic strategies aimed at increasing fetal globin production in diseases such as beta thalassemia and sickle cell anemia by inhibiting BCL11A are currently being explored.
Entrez Gene ID
Human53335
Mouse14025
Zebrafish678650
UniProt ID
HumanQ9H165
MouseQ9QYE3
ZebrafishQ1RLR5
Alternative Names
EVI9; CTIP1; DILOS; ZNF856; HBFQTL5; BCL11A-L; BCL11A-S; BCL11a-M; BCL11A-XL
Function
Transcription factor (PubMed:16704730, PubMed:29606353).
Associated with the BAF SWI/SNF chromatin remodeling complex (PubMed:23644491).
Binds to the 5'-TGACCA-3' sequence motif in regulatory regions of target genes, including a distal promoter of the HBG1 hemoglobin subunit gamma-1 gene (PubMed:29606353).
Involved in regulation of the developmental switch from gamma- to beta-globin, probably via direct repression of HBG1; hence indirectly repressing fetal hemoglobin (HbF) level (PubMed:29606353, PubMed:26375765).
Involved in brain development (PubMed:27453576).
May play a role in hematopoiesis (By similarity).
Essential factor in lymphopoiesis required for B-cell formation in fetal liver (By similarity).
May function as a modulator of the transcriptional repression activity of NR2F2 (By similarity).
Biological Process
Cellular response to L-glutamate Source: Ensembl
Negative regulation of axon extension Source: BHF-UCL
Negative regulation of branching morphogenesis of a nerve Source: Ensembl
Negative regulation of collateral sprouting Source: BHF-UCL
Negative regulation of dendrite development Source: BHF-UCL
Negative regulation of dendrite extension Source: Ensembl
Negative regulation of neuron projection development Source: BHF-UCL
Negative regulation of neuron remodeling Source: Ensembl
Negative regulation of protein homooligomerization Source: BHF-UCL
Negative regulation of transcription by RNA polymerase II Source: ARUK-UCL
Positive regulation of collateral sprouting Source: BHF-UCL
Positive regulation of gene expression Source: Ensembl
Positive regulation of neuron projection development Source: BHF-UCL
Positive regulation of transcription by RNA polymerase II Source: BHF-UCL
Protein sumoylation Source: UniProtKB
Regulation of dendrite development Source: BHF-UCL
Regulation of transcription by RNA polymerase II Source: GO_Central
Cellular Location
Cytoplasm; Nucleus; Chromosome. Associates with the nuclear body. Colocalizes with SUMO1 and SENP2 in nuclear speckles (By similarity).
Isoform 1: Nucleus matrix. Colocalizes with BCL6 in nuclear paraspeckles.
Isoform 2: Cytoplasm; Nucleus. Predominantly localized in the nucleus in nuclear paraspeckles.
Isoform 3: Cytoplasm; Nucleus. Predominantly localized in the cytoplasm in the absence of interaction with isoform 1 and isoform 2. In presence of isoform 1 or isoform 2, translocates from the cytoplasm into nuclear paraspeckles.
Involvement in disease
Chromosomal aberrations involving BCL11A are associated with B-cell malignancies. Translocation t(2;14)(p13;q32.3) causes BCL11A deregulation and overexpression.
Intellectual developmental disorder with persistence of fetal hemoglobin (IDPFH): An autosomal dominant disorder characterized by delayed psychomotor development, intellectual disability, variable dysmorphic features, including microcephaly, downslanting palpebral fissures, strabismus, and external ear abnormalities, and asymptomatic persistence of fetal hemoglobin.
PTM
Sumoylated with SUMO1.
More Infomation
Ask a question We look forward to hearing from you.
0 reviews or Q&As
Loading...
Have you used Mouse Anti-BCL11A Recombinant Antibody (H1)?
Submit a review and get a Coupon or an Amazon gift card. 20% off Coupon $30 eGift Card
Submit a review
Loading...
For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

Learn more

Documents

Online Inquiry