CSRP3 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA529155-Each-of-1 | In Stock | ₹ 49,439.50 |
PIPA529155 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 49,439.50
GST (18%): ₹ 8,899.11
Total Price: ₹ 58,338.61
Antigen
CSRP3
Classification
Polyclonal
Conjugate
Unconjugated
Gene
Csrp3
Gene Alias
cardiac LIM domain protein; cardiac LIM protein; Clp; CMD1M; CMH12; CRP3; Csrp3; cysteine and glycine rich protein 3; cysteine and glycine-rich protein 3; cysteine and glycine-rich protein 3 (cardiac LIM protein); cysteine-rich protein 3; LIM domain only 4; LIM domain protein, cardiac; LMO4; MGC14488; MGC61993; MLP; MMLP; Muscle LIM protein; muscle lim protein isoform
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
13009, 8048
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Concentration
0.8 mg/mL
Formulation
0.1M tris glycine with 10% glycerol and 0.01% thimerosal; pH 7
Gene Accession No.
P50461, P50462
Gene Symbols
Csrp3
Immunogen
Recombinant fragment corresponding to a region within amino acids 1 and 194 of Human CSRP3
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Recommended positive controls: HeLa
- Predicted reactivity: Mouse (97%), Rat (95%), Pig (98%), Chicken (87%), Bovine (96%)
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- This gene encodes a member of the CSRP family of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation
- The LIM/double zinc-finger motif found in this protein is found in a group of proteins with critical functions in gene regulation, cell growth, and somatic differentiation
- Mutations in this gene are thought to cause heritable forms of hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) in humans
- Alternatively spliced transcript variants with different 5' UTR, but encoding the same protein, have been found for this gene.