COMMD10 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA531868-Each-of-1 | In Stock | ₹ 47,036.50 |
PIPA531868 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 47,036.50
GST (18%): ₹ 8,466.57
Total Price: ₹ 55,503.07
Antigen
COMMD10
Classification
Polyclonal
Conjugate
Unconjugated
Gene
COMMD10
Gene Alias
2310003A05Rik; AU019438; COMM domain containing 10; COMM domain-containing protein 10; COMMD10; Down-regulated in W/WV mouse stomach 2; DRWMS2; HSPC305; mDRWMS2; PTD002
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
51397, 69456
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
1 mg/mL
Formulation
PBS with 1% BSA, 20% glycerol and 0.01% thimerosal; pH 7
Gene Accession No.
Q8JZY2, Q9Y6G5
Gene Symbols
COMMD10
Immunogen
Recombinant fragment corresponding to a region within amino acids 1 and 202 of Human COMMD10
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Recommended positive controls: A549, HeLa, HepG2, HCT116
- Predicted reactivity: Mouse (88%), Rat (89%), Pig (92%), Chicken (80%), Bovine (93%)
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- The COMMD family represents a group of evolutionary conserved proteins that share a common COMM domain at their extreme C-terminus, which provides an interface for protein-protein interactions
- COMMD10 (COMM domain containing 10), also known as PTD002 or HSPC305, is a 202 amino acid protein that belongs to the COMMD family and contains one COMM domain
- The gene encoding COMMD10 maps to human chromosome 5, which contains 181 million base pairs and comprises nearly 6% of the human genome
- Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome
- May modulate activity of cullin-RING E3 ubiquitin ligase (CRL) complexes (PubMed:21778237)
- May down-regulate activation of NF-kappa-B.