Rabbit Recombinant Monoclonal RBMY1A1 antibody. Suitable for WB, IHC-P and reacts with Human samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
WB | IHC-P | |
---|---|---|
Human | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/1000 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/4000 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
RNA-binding protein involved in pre-mRNA splicing. Required for sperm development. Acts additively with TRA2B to promote exon 7 inclusion of the survival motor neuron SMN. Binds non-specifically to mRNAs.
RBM1, RBM2, YRRM1, YRRM2, RBMY1A1, RNA-binding motif protein 1, RNA-binding motif protein 2, Y chromosome RNA recognition motif 1, hRBMY
Rabbit Recombinant Monoclonal RBMY1A1 antibody. Suitable for WB, IHC-P and reacts with Human samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Based on sequence analysis, ab200202 recognizes 2 isoforms with the predicted MWs of 56KDa and 51KDa respectively. Sequence analysis also showed a 100% homology with RBY1F, RBY1E, RBY1D, RBY1C and RBY1B.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
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RBMY1A1 also known as RNA-binding motif protein Y chromosome family 1 member A1 is a protein with a molecular mass of about 47 kDa. It is expressed predominantly in the testis playing an important role in male germ cell development. The protein functions mechanically by binding to RNA featuring an RNA recognition motif that facilitates its role in RNA processing. Its localization to the nucleus highlights its function in post-transcriptional regulation.
RBMY1A1 contributes to spermatogenesis by participating in the regulation of RNA splicing and stability. It is part of a larger complex of proteins that associate with RNA impacting gene expression in male germ cells. The protein interacts with other splicing factors influencing the alternative splicing of pre-mRNAs essential for spermatogenic processes. This highlights RBMY1A1's specific role in sperm development and functioning.
The involvement of RBMY1A1 is significant in the mRNA processing pathway. It connects with proteins like hnRNPGT and other spliceosomal components. RBMY1A1’s interaction in this pathway helps in the formation of messenger ribonucleoprotein complexes which are necessary for the maturation and transport of mRNA molecules. Its activity is important in maintaining the integrity of gene expression regulation in spermatogenic cells intertwining with broader pathways of male fertility.
RBMY1A1 has been implicated in cases of azoospermia a condition characterized by the absence of sperm in semen. This condition associates with its critical role in fertility where loss or malfunction correlates with impaired sperm production. Moreover RBMY1A1 has links to testicular germ cell tumors where abnormal expression and mutations have been observed. It also interacts with other proteins like DAZL which is another factor associated with reproductive health emphasizing its relevance in male reproductive disorders.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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Please note lanes 2-5 represent RBMY1A1 negative lysates.
Based on sequence analysis, ab200202 recognizes 2 isoforms with the predicted MWs of 56KDa and 51KDa respectively. Sequence analysis also showed a 100% homology with RBY1F, RBY1E, RBY1D, RBY1C and RBY1B.
Blocking/Dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-RBMY1A1 antibody [R12508(2)] (ab200202) at 1/1000 dilution
Lane 1: Human testis lysate at 10 µg
Lane 2: Human fetal brain tissue lysate at 10 µg
Lane 3: Human fetal heart tissue lysate at 10 µg
Lane 4: Human fetal kidney tissue lysate at 10 µg
Lane 5: Human fetal spleen tissue lysate at 10 µg
All lanes: Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 56 kDa
Observed band size: 51 kDa, 56 kDa
Exposure time: 5s
Immunohistochemical analysis of paraffin-embedded Human testis tissue labeling RBMY1A1 with ab200202 at 1/4000 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution. Nucleus staining of Human testis tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Immunohistochemical analysis of paraffin-embedded Human liver tissue with ab200202 at 1/4000 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution. Counter stained with Hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution.
Please note Human liver tissue represents a RBMY1A1 negative control.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
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