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PIPA519680

IHH Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA519680-Each-of-1 In Stock ₹ 46,235.50

PIPA519680 - Each of 1

₹ 46,235.50

In Stock

Quantity

1

Base Price: ₹ 46,235.50

GST (18%): ₹ 8,322.39

Total Price: ₹ 54,557.89

Antigen

IHH

Classification

Polyclonal

Conjugate

Unconjugated

Gene

Ihh

Gene Alias

BDA1; HHG2; HHG-2; Ihh; Indian hedgehog; Indian hedgehog homolog; indian hedgehog protein; Indian hedgehog protein C-product; Indian hedgehog protein N-product; indian hedgehog protein; LOW QUALITY PROTEIN: indian hedgehog protein; Indian hedgehog signaling molecule; Indian hedgehog-like protein

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

16147, 3549

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

Applications

Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Concentration

0.6 mg/mL

Formulation

PBS with BSA and 0.02% sodium azide; pH 7.4

Gene Accession No.

P97812, Q14623

Gene Symbols

Ihh

Immunogen

Synthetic peptide conjugated to KLH derived from within residues 350 to the C-terminus of Mouse Ihh.

Quantity

100 μg

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG

Description

  • Heat mediated antigen retrieval recommended prior to tissue staining
  • This antibody is predicted to react with cow based on sequence homology
  • Ihh encodes a member of the hedgehog family of secreted signaling molecules
  • Hedgehog proteins are essential regulators of a variety of developmental processes including growth, patterning and morphogenesis
  • The encoded protein specifically plays a role in bone growth an differentiation
  • Mutations in this gene are the cause of brachydactyly type A1 which is characterized by shortening or malformation of the phalanges
  • Mutations in this gene are also the cause of acrocapitofemoral dysplasia.