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FASTKD2 Antibody 8 Publications

Rabbit Polyclonal| Catalog number: 17464-1-AP

Featured Product KD/KO validated

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Con: 61 μg/150 μl

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Tested Applications

Applications:
WB, IP, IF, ELISA
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Images See all

FASTKD2 Antibody WB mouse brain tissue 17464-1-AP

mouse brain tissue were subjected to SDS PAGE followed by western blot with 17464-1-AP(FASTKD2 antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours

FASTKD2 Antibody IF COS7 cells 17464-1-AP

IF result of anti-FASTKD2 (17464-1-AP) with COS7 cells.

FASTKD2 Antibody IP mouse heart tissue 17464-1-AP

IP Result of anti-FASTKD2 (IP:17464-1-AP, 4ug; Detection:17464-1-AP 1:300) with mouse heart tissue lysate 4000ug.

Species specificity:
human, mouse, rat
Positive WB detected in:
mouse brain tissue, mouse heart tissue
Positive IP detected in:
mouse heart tissue
Positive IF detected in:
COS7 cells, U2OS cells
Recommended dilution:
WB : 1:500-1:2000
IP : 0.5-4.0 ug for IP and 1:200-1:1000 for WB
IF : 1:20-1:200
Sample-dependent, check data in Validation tab

Product Information

Source:
Rabbit
Purification method:
Antigen affinity purification
Isotype:
IgG
Storage:
PBS with 0.02% sodium azide and 50% glycerol pH 7.3. Store at -20oC. Aliquoting is unnecessary for -20oC storage.

Immunogen Information

Immunogen:
FASTKD2 fusion protein Ag11314
Full name:
FAST kinase domains 2
Calculated molecular weight:
710aa,81 kDa
Observed molecular weight:
73-75 kDa
GenBank accession number:
BC001544
Gene ID (NCBI):
22868
Gene symbol
FASTKD2
Synonyms
FAST kinase domains 2, FASTKD2, KIAA0971

Background

FASTKD2(FAST kinase domain-containing protein 2) is also named as KIAA0971 and belongs to the FAST kinase family.A potential cleavage site of the 79 kDa FASTKD2 precursor protein by the mitochondrial matrix protease (MMP) is present between M52 and Q53 and predicts the mature imported protein from the FASTKD2 precursor to be composed of 642 amino acid residues for a MW of approximately 73 kDa(PMID: 18771761) and the clinical and MRI findings of the FASTKD2-associated disease are rather unusual for mitochondrial disorders.


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