Mouse Anti-ACTR2 Recombinant Antibody (V2-12516) (CBMAB-1006-CN)
(a-e) Electron microscopy showing elongated spermatid morphology during spermiation in Katnal2WT/WT and Katnal2Y86C/Y86C mice. Detachment of the acrosome (red arrowheads) from the nucleus was frequently observed in Katnal2Y86C/Y86C (b) but not Katnal2WT/WT (a) spermatids. Retention of cytoplasm was frequently seen in Katnal2Y86C/Y86C spermatids that had failed spermiation (c). Within the cytoplasm of retained spermatids, disorganised outer dense fibres (red arrowheads) were frequently observed (c). Ectoplasmic specializations (black arrowheads) showed normal morphology in Katnal2Y86C/Y86C (d) and Katnal2WT/WT (a) spermatids, and were absent in Katnal2Y86C/Y86C retained spermatids (e) indicating they were disassembled normally prior to spermiation. Tubulobulbar complexes (asterisks) were present in Katnal2WT/WT (a) spermatids but were absent in Katnal2Y86C/Y86C spermatids (d). Scale bars in a-e = 1 μm. Immunostaining of seminiferous tubules for the ectoplasmic specialization marker espin confirmed ectoplasmic specialisations were disassembled normally in Katnal2WT/WT and Katnal2Y86C/Y86C spermatids (f-k). Ectoplasmic specializations were present in early step 16 (stage VII) Katnal2WT/WT (f) and Katnal2Y86C/Y86C spermatids (i), but were absent from late step 16 (stage VIII) Katnal2WT/WT (g) and Katnal2Y86C/Y86C spermatids (j) and from retained (stage IX) Katnal2Y86C/Y86C spermatids (k). Immunostaining of seminiferous tubules for the tubulobulbar complex markers dynamin-2 and ARP2 confirmed the absence of tubulobulbar complexes from Katnal2Y86C/Y86C (o-p) but not Katnal2WT/WT (l-m) spermatids. Residual body (arrowheads) formation in Katnal2WT/WT (n) versus Katnal2Y86C/Y86C (q) mice. Residual bodies were absent in Katnal2Y86C/Y86C (q) mice. Scale bars in f-q = 10 μm. ...View More
Basic Information
| Application | Note |
| IF(ICC) | 10 μg/ml |
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Associative learning
Asymmetric cell division
Cellular response to interferon-gamma
Cellular response to trichostatin A
Cilium assembly
Cytosolic transport
Ephrin receptor signaling pathway
Establishment or maintenance of cell polarity
Fc-gamma receptor signaling pathway involved in phagocytosis
Meiotic chromosome movement towards spindle pole
Meiotic cytokinesis
Membrane organization
Neutrophil degranulation
Positive regulation of dendritic spine morphogenesis
Positive regulation of double-strand break repair via homologous recombination
Positive regulation of lamellipodium assembly
Positive regulation of transcription by RNA polymerase II
Response to ethanol
Response to immobilization stress
Spindle localization
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Please try the standard protocols which include: protocols, troubleshooting and guide.
Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme Linked Immunospot (ELISpot)
Proteogenomic
Other Protocols
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.).
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