Anti-SYCE1 Antibody

$99.00$319.00

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

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Rabbit Anti-SYCE1 Antibody (CSB-PA022987ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Synaptonemal complex central element protein 1 Antibody,Cancer/testis antigen 76 Antibody,CT76 Antibody,SYCE1 Antibody,C10orf94 Antibody

More alternative names for the antibody
bA108K14.6 antibody|C10orf94 antibody|Cancer/testis antigen 76 antibody|CT76 antibody|RP11-108K14.6 antibody|Syce1 antibody|SYCE1_HUMAN antibody|Synaptonemal complex central element protein 1 antibody
Anti-SYCE1 antibody (ab122634)
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Recommended applications: ELISA, WB, IHC

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-SYCE1 Antibody

Catalogue No.

CSB-PA022987ESR2HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Synaptonemal complex central element protein 1 protein (132-351AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

39 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:93426( Human), Omim:611486( Human), SwissProt:Q8N0S2 ( Human), Unigene:553795( Human)

Protein function

Major component of the transverse central element of synaptonemal complexes (SCS), formed between homologous chromosomes during meiotic prophase. Requires SYCP1 in order to be incorporated into the central element. May have a role in the synaptonemal complex assembly, stabilization and recombination. .

Involvement in disease

Premature ovarian failure 12 (POF12) [MIM:616947]: An ovarian disorder defined as the cessation of ovarian function under the age of 40 years. It is characterized by oligomenorrhea or amenorrhea, in the presence of elevated levels of serum gonadotropins and low estradiol. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Spermatogenic failure, 15 (SPGF15) [MIM:616950]: An infertility disorder caused by spermatogenesis defects and characterized by non-obstructive azoospermia due to complete meiotic maturation arrest. SPGF15 inheritance is autosomal recessive. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the SYCE family.

Protein cellular localization

Nucleus . Chromosome . Note=Associates with chromatin. In prophase I stage of meiosis, localizes in the transverse central elements of the central region between lateral elements of the synaptonemal complexes. Found only where the chromosome cores are synapsed. Colocalizes with SYCE2 in the central elements. .

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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