PIPA568352
TMC7 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA568352-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA568352 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
TMC7
Classification
Polyclonal
Conjugate
Unconjugated
Gene
TMC7
Gene Alias
1700030H01Rik; C230064B05; C630024K23Rik; RGD1564267; Tmc7; transmembrane channel like 7; transmembrane channel-like 7; transmembrane channel-like gene family 7; transmembrane channel-like protein 7
Host Species
Rabbit
Purification Method
affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
209760, 499254, 79905
Content And Storage
-20°C
Form
Liquid
Applications
Western Blot
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Gene Accession No.
Q7Z402, Q8C428
Gene Symbols
TMC7
Immunogen
Synthesized peptide derived from human TMC7.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Predicted to react with Mouse and Rat samples
- TMC7 (Transmembrane channel-like protein 7) is a 723 amino acid protein that is a member of the TMC protein family
- All TMC genes encode transmembrane proteins with intracellular amino- and carboxy- termini and at least eight membrane spanning domains
- Therefore, TMC7 is a multi-pass membrane protein that may regulate or function as an ion channel or transporter
- The gene encoding TMC7 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome
- The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth
- The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.