SPTA1 Polyclonal antibody

SPTA1 Polyclonal Antibody for WB, IF-P, FC (Intra), ELISA
Cat No. 55227-1-AP

Host / Isotype

Rabbit / IgG

Reactivity

human, rat

Applications

WB, IF-P, FC (Intra), ELISA

EL2, Alpha I spectrin

Formulation:  PBS and Azide
PBS and Azide
Conjugate:  Unconjugated
Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

Please visit your regions distributor:


Tested Applications

Positive WB detected inrat red blood cells, human blood
Positive IF-P detected inmouse lung tissue
Positive FC (Intra) detected inK-562 cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:200-1:1000
Immunofluorescence (IF)-PIF-P : 1:50-1:500
Flow Cytometry (FC) (INTRA)FC (INTRA) : 0.40 ug per 10^6 cells in a 100 µl suspension
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

55227-1-AP targets SPTA1 in WB, IF-P, FC (Intra), ELISA applications and shows reactivity with human, rat samples.

Tested Reactivity human, rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Peptide Predict reactive species
Full Name spectrin, alpha, erythrocytic 1 (elliptocytosis 2)
Calculated Molecular Weight 280 kDa
Observed Molecular Weight 280 kDa
GenBank Accession NumberNM_003126
Gene Symbol SPTA1
Gene ID (NCBI) 6708
RRIDAB_3086436
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
UNIPROT IDP02549
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol , pH 7.3
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

Alpha 1 Spectrin also known as SPTA1, EL2, belongs to the spectrin family. Spectrin is the major constituent of the cytoskeletal network underlying the erythrocyte plasma membrane. It associates with band 4.1 and actin to form the cytoskeletal superstructure of the erythrocyte plasma membrane. Mutations in SPTA1 result in a variety of hereditary red blood cell disorders, including elliptocytosis-2, pyropoikilocytosis, and spherocytosis, type 3(PMID: 1541680, 8941647).

Protocols

Product Specific Protocols
WB protocol for SPTA1 antibody 55227-1-APDownload protocol
IF protocol for SPTA1 antibody 55227-1-APDownload protocol
FC protocol for SPTA1 antibody 55227-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols
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