Anti-TPK1 Antibody

$99.00$319.00

Reactivity: Human,Mouse
Applications: ELISA,WB,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-TPK1 Antibody (CSB-PA024103ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Thiamin pyrophosphokinase 1 Antibody,hTPK1 Antibody,Placental protein 20 Antibody,PP20 Antibody,Thiamine pyrophosphokinase 1 Antibody,TPK1 Antibody

More alternative names for the antibody
hTPK1 antibody|Placental protein 20 antibody|PP20 antibody|Thiamin pyrophosphokinase 1 antibody|Thiamine diphosphokinase antibody|Thiamine kinase antibody|Thiamine pyrophosphokinase 1 antibody|THMD5 antibody|TPK1 antibody|TPK1_HUMAN antibody
Anti-TPK1 antibody [EPR10918] (ab170863)
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Recommended applications: ELISA, WB, IHC

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-TPK1 Antibody

Catalogue No.

CSB-PA024103ESR2HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Thiamin pyrophosphokinase 1 protein (1-243AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

27 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:788066( Cow), Entrez Gene:27010( Human), Entrez Gene:29807( Mouse), Entrez Gene:680668( Rat), Omim:606370( Human), SwissProt:Q5E9T4( Cow), SwissProt:Q9H3S4( Human), SwissProt:Q9R0M5( Mouse), Unigene:660232( Human), Unigene:320979( Mouse), Unigene:215836( Rat)

Protein function

Catalyzes the phosphorylation of thiamine to thiamine pyrophosphate. Can also catalyze the phosphorylation of pyrithiamine to pyrithiamine pyrophosphate. .

Protein tissue specificity

Detected in heart, kidney, testis, small intestine and peripheral blood leukocytes, and at very low levels in a variety of tissues. .

Involvement in disease

Thiamine metabolism dysfunction syndrome 5, episodic encephalopathy type (THMD5) [MIM:614458]: An autosomal recessive metabolic disorder due to an inborn error of thiamine metabolism. The phenotype is highly variable, but in general, affected individuals have onset in early childhood of acute encephalopathic episodes associated with increased serum and CSF lactate. These episodes result in progressive neurologic dysfunction manifest as gait disturbances, ataxia, dystonia, and spasticity, which in some cases may result in loss of ability to walk. Cognitive function is usually preserved, although mildly delayed development has been reported. These episodes are usually associated with infection and metabolic decompensation. Some patients may have recovery of some neurologic deficits. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the thiamine pyrophosphokinase family.

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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