RSRC1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5110332-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA5110332 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
RSRC1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
RSRC1
Gene Alias
1200013F24Rik; arginine and serine rich coiled-coil 1; arginine/serine-rich coiled coil protein 1; arginine/serine-rich coiled-coil 1; arginine/serine-rich coiled-coil protein 1; BM-011; RGD1304968; Rsrc1; Serine/Arginine-related protein 53; SFRS21; splicing factor, arginine/serine-rich 21; Srrp53
Host Species
Rabbit
Purification Method
Affinity Chromatography
Regulatory Status
RUO
Gene ID (Entrez)
361956, 51319, 66880
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles
Form
Liquid
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Concentration
0.3 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3
Gene Accession No.
Q5PPJ2, Q96IZ7, Q9DBU6
Gene Symbols
RSRC1
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 117-276 of human RSRC1 (NP_001258763.1).
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Immunogen sequence: EHLPPAEQAK ARLQLVLEAA AKADEALKAK ERNEEEAKRR KEEDQATLVE QVKRVKEIEA IESDSFVQQT FRSSKEVKKS VEPSEVKQAT STSGPASAVA DPPSTEKEID PTSIPTAIKY QDDNSLAHPN LFIEKADAEE KWFKRLIALR QERLMGSPVA RSRC1 is a gene that encodes a protein belonging to the serine and arginine rich-related protein family
- This protein plays a crucial role in both constitutive and alternative mRNA splicing
- Research suggests that this gene may be linked to schizophrenia, and a pseudogene of RSRC1 is present on chromosome 9
- Alternative splicing of RSRC1 leads to the formation of multiple transcript variants that encode distinct isoforms
- Additionally, RSRC1 has been associated with various disorders, including Autosomal Recessive Non-Syndromic Intellectual Disability and Intellectual Developmental Disorder, Autosomal Recessive 70.