HAX1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA584982-Each-of-1 | In Stock | ₹ 48,905.50 |
PIPA584982 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 48,905.50
GST (18%): ₹ 8,802.99
Total Price: ₹ 57,708.49
Antigen
HAX1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
Hax1
Gene Alias
FLJ17042, FLJ18492, FLJ93803, Hax1, HAX-1, HCLS1 (and PKD2) associated protein, HCLS1 associated protein X-1, HCLS1 associated X-1, HCLS1-associated protein X-1, HCLSBP1, HS1 binding protein, HS1-associated protein X-1, HS1-associating protein X-1, HS1-binding protein 1, HS1BP1, HSP1BP-1, mHAX-1s, OTTHUMP00000034190, RP11-137P24.1, SCN3, SIG-111, Silg111
Host Species
Rabbit
Purification Method
Anitgen affinity chromatography, Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
10456
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, Western Blot, Western Blot
Concentration
0.05 mg/mL
Formulation
PBS with 40% glycerol and 0.02% sodium azide, pH 7.2
Gene Accession No.
O00165
Gene Symbols
Hax1
Immunogen
Recombinant protein corresponding to Human HAX1
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Immunogen sequence: LGPVLQPQPK SYFKSISVTK ITKPDGIVEE RRTVVDSEGR TETTVTRHEA The protein encoded by this gene is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases
- It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin
- It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body
- Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease
- Two transcript variants encoding different isoforms have been found for this gene.