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Western blot analysis of extracts of various cell lines, using α-Actin-1 (ATCA1) Rabbit mAb (A2235) at 1:1000 dilution.|Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.|Lysates/proteins: 25ug per lane.|Blocking buffer: 3% nonfat dry milk in TBST.|Detection: ECL Basic Kit (RM00020).|Exposure time: 1s.
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Immunohistochemistry of paraffin-embedded rat lung using α-Actin-1 (ATCA1) Rabbit mAb (A2235) at dilution of 1:100 (40x lens).
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Immunohistochemistry of paraffin-embedded human appendix using α-Actin-1 (ATCA1) Rabbit mAb (A2235) at dilution of 1:100 (40x lens).
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Immunohistochemistry of paraffin-embedded mouse heart using α-Actin-1 (ATCA1) Rabbit mAb (A2235) at dilution of 1:100 (40x lens).
α-Actin-1 (ATCA1) Rabbit mAb
Catalog No：AB-A2235
Manufacturer：ABclonal
Synonyms：ACTA, ASMA, CFTD, CFTD1, CFTDM, MPFD, NEM1, NEM2, NEM3, SHPM
Applications：WB,IHC,IF
Reactivity：Human,Mouse,Rat
Host：Rabbit
Conjugate：No
€65,00 – €485,00
| Product Name: | 伪-Actin-1 (ATCA1) Rabbit mAb |
| Category: | Monoclonal Antibodies |
| Description: | The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects. [provided by RefSeq, Jul 2008] |
| Immunogen: | A synthesized peptide derived from human 伪-Actin-1 (ATCA1) |
| Gene ID: | 58 |
| Swiss prot: | P68133 |
| Molecular weight: | 42kDa |
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