PIPA5114170

DGCR6L Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5114170-Each-of-1 In Stock ₹ 46,502.50

PIPA5114170 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

DGCR6L

Classification

Polyclonal

Conjugate

Unconjugated

Gene

DGCR6L

Gene Alias

DGCR6; DGCR6L; DiGeorge syndrome critical region 6-like protein; DiGeorge syndrome critical region gene 6 like; DiGeorge syndrome critical region gene 6-like; protein DGCR6L

Host Species

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

85359

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Applications

Western Blot

Concentration

0.5 mg/mL

Formulation

PBS with 2% sucrose and 0.09% sodium azide

Gene Accession No.

Q9BY27

Gene Symbols

DGCR6L

Immunogen

Synthetic peptide directed towards the C terminal region of human DGCR6L

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

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Description

  • Immunogen sequence: QQRELEAVEH RIREEQRAMD QKIILELDRK VADQQSTLEK AGVAGFYVTT For short term use, store at 2-8°C up to 1 week
  • For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles
  • Predicted homology: Cow: 100%; Dog: 100%; Guinea Pig: 100%; Horse: 100%; Human: 100%; Mouse: 100%; Rabbit: 100%; Rat: 100% This gene, the result of a duplication at this locus, is one of two functional genes encoding nearly identical proteins that have similar expression patterns
  • The product of this gene is a protein that shares homology with the Drosophila gonadal protein, expressed in gonadal tissues and germ cells, and with the human laminin gamma-1 chain that functions in cell attachment and migration
  • This gene is located in a region of chromosome 22 implicated in the DiGeorge syndrome, one facet of a broader collection of anomalies referred to as the CATCH 22 syndrome
  • [provided by RefSeq].