HOXD10 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA519007-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA519007 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
HOXD10
Classification
Polyclonal
Conjugate
Unconjugated
Gene
HOXD10
Gene Alias
AI385591; AI874987; d10; homeo box 4D; homeo box D10; homeo box D10a; homeobox D10; homeobox D10a; homeobox gene D-10; homeobox protein Hox-4.5; Homeobox protein Hox-4D; homeobox protein Hox-4E; Homeobox protein Hox-5.3; homeobox protein Hox-C10; Homeobox protein Hox-D10; homeobox protein Hox-D10a; homeobox protein Hox-D11; homeobox protein Hox-D10; HOX4; Hox-4.4; Hox-4.5; Hox-45; HOX4D; HOX4E; Hox-5.3; hoxc10; hox-C10; Hoxc10 protein; Hoxd10; HOX-D10; hoxd-10; hoxd10a; hoxd10a protein; z-82
Host Species
Goat
Purification Method
Ammonium sulfate precipitation
Regulatory Status
RUO
Gene ID (Entrez)
3236
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles
Form
Liquid
Applications
Flow Cytometry, Immunohistochemistry, Western Blot
Concentration
0.5 mg/mL
Formulation
TBS with 0.5% BSA and 0.02% sodium azide; pH 7.3
Gene Accession No.
P28358
Gene Symbols
HOXD10
Immunogen
Synthetic peptide sequence (PNRSCRIEQPVTQQ) corresponding to the internal amino acids of HOXD10
Quantity
100 μg
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- This antibody is predicted to react with bovine, equine, mouse and rat based on sequence homology
- This antibody is tested in Peptide ELISA: antibody detection limit dilution 32,000
- This gene is a member of the Abd-B homeobox family and encodes a protein with a homeobox DNA-binding domain
- It is included in a cluster of homeobox D genes located on chromosome 2
- The encoded nuclear protein functions as a sequence-specific transcription factor that is expressed in the developing limb buds and is involved in differentiation and limb development
- Mutations in this gene have been associated with Wilm's tumor and congenital vertical talus and/or a foot deformity resembling that seen in Charcot-Marie-Tooth disease.