C12orf57 Antibody

Datasheet

Code	CSB-PA859105LA01HU
Size	US$166
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Product Details
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Target Background

Product Details

Full Product Name

Rabbit anti-Homo sapiens (Human) C12orf57 Polyclonal antibody

Uniprot No.

Q99622

Target Names

C12orf57

Alternative Names

C10_HUMAN antibody; C12orf57 antibody; Protein C10 antibody

Raised in

Rabbit

Species Reactivity

Human

Immunogen

Recombinant Human Protein C10 protein (2-126AA)

Immunogen Species

Homo sapiens (Human)

Conjugate

Non-conjugated

The C12orf57 Antibody (Product code: CSB-PA859105LA01HU) is Non-conjugated. For C12orf57 Antibody with conjugates, please check the following table.

Conjugate	Product Code	Product Name	Application
HRP	CSB-PA859105LB01HU	C12orf57 Antibody, HRP conjugated	ELISA
FITC	CSB-PA859105LC01HU	C12orf57 Antibody, FITC conjugated
Biotin	CSB-PA859105LD01HU	C12orf57 Antibody, Biotin conjugated	ELISA

Clonality

Polyclonal

Isotype

IgG

Purification Method

>95%, Protein G purified

Concentration

It differs from different batches. Please contact us to confirm it.

Buffer

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4

Form

Liquid

Tested Applications

ELISA

Protocols

ELISA Protocol

Troubleshooting and FAQs

Antibody FAQs

Storage

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Lead Time

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

Usage

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

Customer Reviews and Q&A

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Target Background

Function

In brain, may be required for corpus callosum development.

Gene References into Functions

Exome sequencing identifies compound heterozygous mutations in C12orf57 in two siblings with severe intellectual disability, hypoplasia of the corpus callosum, chorioretinal coloboma, and intractable seizures. PMID: 24798461
The findings strongly support the candidacy of C12orf57 as a gene that is mutated in a distinct syndromic form of colobomatous microphthalmia in humans. PMID: 23453665

Involvement in disease

Temtamy syndrome (TEMTYS)

Subcellular Location

Cytoplasm.

Protein Families

UPF0456 family

Tissue Specificity

Ubiquitously expressed, with higher expression in lung and fetal brain.

Database Links

HGNC: 29521

OMIM: 218340

KEGG: hsa:113246

STRING: 9606.ENSP00000229281

UniGene: Hs.405913

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Antibody FAQs What Is an Antibody? How to Choose an Antibody for Scientific Research? The difference between primary antibody and secondary antibod The Meaning of Irregular Antibody Screening Tag Antibodies, Your Good Partner in Protein Research How to Choose the Loading Control Antibodies?

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301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)

[email protected]

Address

7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA

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